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nsv6910062

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:114,216

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 473 SVs from 66 studies. See in: genome view    
    Submitted genomic6,758,184-6,872,399Question Mark
    Overlapping variant regions from other studies: 473 SVs from 66 studies. See in: genome view    
    Remapped(Score: Perfect):6,779,415-6,893,630Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6910062Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr116,758,1846,872,399
    nsv6910062RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr116,779,4156,893,630

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18353119deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18353119Submitted genomicNC_000011.10:g.675
    8184_6872399del
    GRCh38 (hg38)NC_000011.10Chr116,758,1846,872,399
    nssv18353119RemappedPerfectNC_000011.9:g.6779
    415_6893630del
    GRCh37.p13First PassNC_000011.9Chr116,779,4156,893,630

    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)
    nssv183531192.1e-056276240
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