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nsv7042777

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,332,033

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 9718 SVs from 83 studies. See in: genome view    
    Submitted genomic127,009,007-134,341,039Question Mark
    Overlapping variant regions from other studies: 9725 SVs from 83 studies. See in: genome view    
    Remapped(Score: Good):126,142,990-133,475,069Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7042777Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX127,009,007134,341,039
    nsv7042777RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX126,142,990133,475,069

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765356inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765356Submitted genomicNC_000023.11:g.127
    009007_134341039in
    v
    GRCh38 (hg38)NC_000023.11ChrX127,009,007134,341,039
    nssv18765356RemappedGoodNC_000023.10:g.126
    142990_133475069in
    v
    GRCh37.p13First PassNC_000023.10ChrX126,142,990133,475,069

    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)
    nssv187653561.4e-053214286
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