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nsv6447760

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:867

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 399 SVs from 40 studies. See in: genome view    
    Submitted genomic137,424,583-137,425,449Question Mark
    Overlapping variant regions from other studies: 399 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):140,319,035-140,319,901Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6447760Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9137,424,583137,425,449
    nsv6447760RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9140,319,035140,319,901

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18176419deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18176419Submitted genomicNC_000009.12:g.137
    424583_137425449de
    l
    GRCh38 (hg38)NC_000009.12Chr9137,424,583137,425,449
    nssv18176419RemappedPerfectNC_000009.11:g.140
    319035_140319901de
    l
    GRCh37.p13First PassNC_000009.11Chr9140,319,035140,319,901

    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)
    nssv18176419<0.0011035708
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