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nsv6640639

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:16,627

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 640 SVs from 52 studies. See in: genome view    
    Submitted genomic1,158,973-1,175,599Question Mark
    Overlapping variant regions from other studies: 640 SVs from 52 studies. See in: genome view    
    Remapped(Score: Perfect):1,094,353-1,110,979Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6640639Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr11,158,9731,175,599
    nsv6640639RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr11,094,3531,110,979

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18347138deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18347138Submitted genomicNC_000001.11:g.115
    8973_1175599del
    GRCh38 (hg38)NC_000001.11Chr11,158,9731,175,599
    nssv18347138RemappedPerfectNC_000001.10:g.109
    4353_1110979del
    GRCh37.p13First PassNC_000001.10Chr11,094,3531,110,979

    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)
    nssv183471384e-061276214
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