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nsv6763625

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,263

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 75 SVs from 19 studies. See in: genome view    
    Submitted genomic38,572,515-38,575,777Question Mark
    Overlapping variant regions from other studies: 75 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):38,572,617-38,575,879Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6763625Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr538,572,51538,575,777
    nsv6763625RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr538,572,61738,575,879

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18514708deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18514708Submitted genomicNC_000005.10:g.385
    72515_38575777del
    GRCh38 (hg38)NC_000005.10Chr538,572,51538,575,777
    nssv18514708RemappedPerfectNC_000005.9:g.3857
    2617_38575879del
    GRCh37.p13First PassNC_000005.9Chr538,572,61738,575,879

    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)
    nssv185147081.1e-053275796
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