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nsv7068279

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,584,077

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 4369 SVs from 106 studies. See in: genome view    
    Submitted genomic36,238,268-37,822,344Question Mark
    Overlapping variant regions from other studies: 4376 SVs from 106 studies. See in: genome view    
    Remapped(Score: Perfect):36,238,265-37,822,341Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7068279Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr936,238,26837,822,344
    nsv7068279RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr936,238,26537,822,341

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18783933inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18783933Submitted genomicNC_000009.12:g.362
    38268_37822344inv
    GRCh38 (hg38)NC_000009.12Chr936,238,26837,822,344
    nssv18783933RemappedPerfectNC_000009.11:g.362
    38265_37822341inv
    GRCh37.p13First PassNC_000009.11Chr936,238,26537,822,341

    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)
    nssv187839330.0071861268420
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