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nsv6803144

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,025

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 182 SVs from 32 studies. See in: genome view    
    Submitted genomic1,609,465-1,613,489Question Mark
    Overlapping variant regions from other studies: 182 SVs from 32 studies. See in: genome view    
    Remapped(Score: Perfect):1,649,101-1,653,125Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6803144Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr71,609,4651,613,489
    nsv6803144RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr71,649,1011,653,125

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18537827deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18537827Submitted genomicNC_000007.14:g.160
    9465_1613489del
    GRCh38 (hg38)NC_000007.14Chr71,609,4651,613,489
    nssv18537827RemappedPerfectNC_000007.13:g.164
    9101_1653125del
    GRCh37.p13First PassNC_000007.13Chr71,649,1011,653,125

    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)
    nssv185378274e-061276188
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