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nsv6968676

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,742

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 145 SVs from 26 studies. See in: genome view    
    Submitted genomic96,334,603-96,337,344Question Mark
    Overlapping variant regions from other studies: 145 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):96,877,832-96,880,573Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6968676Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1596,334,60396,337,344
    nsv6968676RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1596,877,83296,880,573

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18398567deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18398567Submitted genomicNC_000015.10:g.963
    34603_96337344del
    GRCh38 (hg38)NC_000015.10Chr1596,334,60396,337,344
    nssv18398567RemappedPerfectNC_000015.9:g.9687
    7832_96880573del
    GRCh37.p13First PassNC_000015.9Chr1596,877,83296,880,573

    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)
    nssv183985674e-061275676
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