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nsv6906752

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65,080

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 700 SVs from 86 studies. See in: genome view    
    Submitted genomic4,901,337-4,966,416Question Mark
    Overlapping variant regions from other studies: 700 SVs from 86 studies. See in: genome view    
    Remapped(Score: Perfect):4,922,567-4,987,646Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6906752Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr114,901,3374,966,416
    nsv6906752RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr114,922,5674,987,646

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18350393deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18350393Submitted genomicNC_000011.10:g.490
    1337_4966416del
    GRCh38 (hg38)NC_000011.10Chr114,901,3374,966,416
    nssv18350393RemappedPerfectNC_000011.9:g.4922
    567_4987646del
    GRCh37.p13First PassNC_000011.9Chr114,922,5674,987,646

    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)
    nssv183503934e-061276076
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