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nsv7064991

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,137,670

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2554 SVs from 79 studies. See in: genome view    
    Submitted genomic122,266,535-123,404,204Question Mark
    Overlapping variant regions from other studies: 2555 SVs from 79 studies. See in: genome view    
    Remapped(Score: Perfect):123,278,774-124,416,444Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7064991Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8122,266,535123,404,204
    nsv7064991RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8123,278,774124,416,444

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18784452inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18784452Submitted genomicNC_000008.11:g.122
    266535_123404204in
    v
    GRCh38 (hg38)NC_000008.11Chr8122,266,535123,404,204
    nssv18784452RemappedPerfectNC_000008.10:g.123
    278774_124416444in
    v
    GRCh37.p13First PassNC_000008.10Chr8123,278,774124,416,444

    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)
    nssv187844524e-061276268
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