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nsv6453002

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:95,848

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 252 SVs from 49 studies. See in: genome view    
    Submitted genomic100,512,435-100,608,282Question Mark
    Overlapping variant regions from other studies: 252 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):102,272,192-102,368,039Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6453002Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10100,512,435100,608,282
    nsv6453002RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10102,272,192102,368,039

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18196192duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18196192Submitted genomicNC_000010.11:g.100
    512435_100608282du
    p
    GRCh38 (hg38)NC_000010.11Chr10100,512,435100,608,282
    nssv18196192RemappedPerfectNC_000010.10:g.102
    272192_102368039du
    p
    GRCh37.p13First PassNC_000010.10Chr10102,272,192102,368,039

    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)
    nssv18196192<0.001139290
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