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nsv6976635

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19,813

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 619 SVs from 70 studies. See in: genome view    
    Submitted genomic768,102-787,914Question Mark
    Overlapping variant regions from other studies: 619 SVs from 70 studies. See in: genome view    
    Remapped(Score: Perfect):818,102-837,914Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6976635Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr16768,102787,914
    nsv6976635RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr16818,102837,914

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18404623deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18404623Submitted genomicNC_000016.10:g.768
    102_787914del
    GRCh38 (hg38)NC_000016.10Chr16768,102787,914
    nssv18404623RemappedPerfectNC_000016.9:g.8181
    02_837914del
    GRCh37.p13First PassNC_000016.9Chr16818,102837,914

    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)
    nssv184046234e-061276244
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