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nsv6568941

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,943,592

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 7070 SVs from 107 studies. See in: genome view    
    Submitted genomic120,593,241-123,536,832Question Mark
    Overlapping variant regions from other studies: 7070 SVs from 107 studies. See in: genome view    
    Remapped(Score: Perfect):120,914,387-123,857,977Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6568941Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6120,593,241123,536,832
    nsv6568941RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6120,914,387123,857,977

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18269236inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18269236Submitted genomicNC_000006.12:g.120
    593241_123536832in
    v
    GRCh38 (hg38)NC_000006.12Chr6120,593,241123,536,832
    nssv18269236RemappedPerfectNC_000006.11:g.120
    914387_123857977in
    v
    GRCh37.p13First PassNC_000006.11Chr6120,914,387123,857,977

    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)
    nssv18269236<0.001139304
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