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nsv6780483

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,538

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 82 SVs from 24 studies. See in: genome view    
    Submitted genomic172,373,837-172,386,374Question Mark
    Overlapping variant regions from other studies: 82 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):171,800,841-171,813,378Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6780483Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5172,373,837172,386,374
    nsv6780483RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5171,800,841171,813,378

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18510896deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18510896Submitted genomicNC_000005.10:g.172
    373837_172386374de
    l
    GRCh38 (hg38)NC_000005.10Chr5172,373,837172,386,374
    nssv18510896RemappedPerfectNC_000005.9:g.1718
    00841_171813378del
    GRCh37.p13First PassNC_000005.9Chr5171,800,841171,813,378

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv185108964e-061276252
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