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nsv7051359

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,812

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 150 SVs from 27 studies. See in: genome view    
    Submitted genomic113,924,805-113,939,616Question Mark
    Overlapping variant regions from other studies: 150 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):114,245,969-114,260,780Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7051359Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6113,924,805113,939,616
    nsv7051359RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6114,245,969114,260,780

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18778278inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18778278Submitted genomicNC_000006.12:g.113
    924805_113939616in
    v
    GRCh38 (hg38)NC_000006.12Chr6113,924,805113,939,616
    nssv18778278RemappedPerfectNC_000006.11:g.114
    245969_114260780in
    v
    GRCh37.p13First PassNC_000006.11Chr6114,245,969114,260,780

    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)
    nssv187782784e-061276268
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