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nsv6915617

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:28,438

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 179 SVs from 37 studies. See in: genome view    
    Submitted genomic96,206,355-96,234,792Question Mark
    Overlapping variant regions from other studies: 179 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):95,939,519-95,967,956Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6915617Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1196,206,35596,234,792
    nsv6915617RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1195,939,51995,967,956

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18355083deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18355083Submitted genomicNC_000011.10:g.962
    06355_96234792del
    GRCh38 (hg38)NC_000011.10Chr1196,206,35596,234,792
    nssv18355083RemappedPerfectNC_000011.9:g.9593
    9519_95967956del
    GRCh37.p13First PassNC_000011.9Chr1195,939,51995,967,956

    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)
    nssv183550834e-061276060
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