{
  "accession": "GCF_000001405.40",
  "current_accession": "GCF_000001405.40",
  "paired_accession": "GCA_000001405.29",
  "tax_id": 9606,
  "organism_name": "Homo sapiens",
  "common_name": "human",
  "assembly_name": "GRCh38.p14",
  "synonym": "hg38",
  "assembly_level": "Chromosome",
  "assembly_status": "current",
  "assembly_type": "haploid-with-alt-loci",
  "refseq_category": "reference genome",
  "release_date": "2022-02-03",
  "paired_assembly": {
    "accession": "GCA_000001405.29",
    "status": "current",
    "only_genbank": "4 unlocalized and unplaced scaffolds",
    "manual_diff": "RefSeq dropped two scaffolds that are predominantly rodent or bacterial in origin (KI270752.1/NT_187507.1 and KI270825.1/NT_187580.1), and dropped two unlocalized scaffolds that are now thought to be redundant with assembled chromosome sequence (KI270721.1/NT_187376.1 and KI270734.1/NT_187389.1)",
    "refseq_genbank_are_different": true,
    "differences": "Removed 4 unlocalized and unplaced scaffolds; RefSeq dropped two scaffolds that are predominantly rodent or bacterial in origin (KI270752.1/NT_187507.1 and KI270825.1/NT_187580.1), and dropped two unlocalized scaffolds that are now thought to be redundant with assembled chromosome sequence (KI270721.1/NT_187376.1 and KI270734.1/NT_187389.1)"
  }
}