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nsv6916077

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:398,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 973 SVs from 65 studies. See in: genome view    
    Submitted genomic124,575,701-124,974,400Question Mark
    Overlapping variant regions from other studies: 973 SVs from 65 studies. See in: genome view    
    Remapped(Score: Perfect):124,445,597-124,844,296Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6916077Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11124,575,701124,974,400
    nsv6916077RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11124,445,597124,844,296

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18578851duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18578851Submitted genomicNC_000011.10:g.124
    575701_124974400du
    p
    GRCh38 (hg38)NC_000011.10Chr11124,575,701124,974,400
    nssv18578851RemappedPerfectNC_000011.9:g.1244
    45597_124844296dup
    GRCh37.p13First PassNC_000011.9Chr11124,445,597124,844,296

    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)
    nssv185788518e-0522269546
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