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nsv7077787

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,520,189

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4235 SVs from 103 studies. See in: genome view    
    Submitted genomic36,095,897-37,616,085Question Mark
    Overlapping variant regions from other studies: 4242 SVs from 103 studies. See in: genome view    
    Remapped(Score: Perfect):36,095,894-37,616,082Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7077787Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr936,095,89737,616,085
    nsv7077787RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr936,095,89437,616,082

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18783931inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18783931Submitted genomicNC_000009.12:g.360
    95897_37616085inv
    GRCh38 (hg38)NC_000009.12Chr936,095,89737,616,085
    nssv18783931RemappedPerfectNC_000009.11:g.360
    95894_37616082inv
    GRCh37.p13First PassNC_000009.11Chr936,095,89437,616,082

    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)
    nssv187839314e-0511269320
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