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nsv7062544

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:194,108

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 864 SVs from 73 studies. See in: genome view    
    Submitted genomic129,540,381-129,734,488Question Mark
    Overlapping variant regions from other studies: 864 SVs from 73 studies. See in: genome view    
    Remapped(Score: Perfect):132,302,660-132,496,767Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7062544Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9129,540,381129,734,488
    nsv7062544RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9132,302,660132,496,767

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18784772inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18784772Submitted genomicNC_000009.12:g.129
    540381_129734488in
    v
    GRCh38 (hg38)NC_000009.12Chr9129,540,381129,734,488
    nssv18784772RemappedPerfectNC_000009.11:g.132
    302660_132496767in
    v
    GRCh37.p13First PassNC_000009.11Chr9132,302,660132,496,767

    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)
    nssv187847724e-061276268
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