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nsv7050777

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,164,933

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 11064 SVs from 107 studies. See in: genome view    
    Submitted genomic117,420,323-122,585,255Question Mark
    Overlapping variant regions from other studies: 11065 SVs from 107 studies. See in: genome view    
    Remapped(Score: Perfect):118,177,899-123,342,831Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7050777Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2117,420,323122,585,255
    nsv7050777RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2118,177,899123,342,831

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767597inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767597Submitted genomicNC_000002.12:g.117
    420323_122585255in
    v
    GRCh38 (hg38)NC_000002.12Chr2117,420,323122,585,255
    nssv18767597RemappedPerfectNC_000002.11:g.118
    177899_123342831in
    v
    GRCh37.p13First PassNC_000002.11Chr2118,177,899123,342,831

    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)
    nssv187675973.6e-0510274882
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