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nsv6454632

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:565,548

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1604 SVs from 75 studies. See in: genome view    
    Submitted genomic8,508,061-9,073,608Question Mark
    Overlapping variant regions from other studies: 1604 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):8,550,024-9,115,571Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6454632Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr108,508,0619,073,608
    nsv6454632RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr108,550,0249,115,571

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18194369duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18194369Submitted genomicNC_000010.11:g.850
    8061_9073608dup
    GRCh38 (hg38)NC_000010.11Chr108,508,0619,073,608
    nssv18194369RemappedPerfectNC_000010.10:g.855
    0024_9115571dup
    GRCh37.p13First PassNC_000010.10Chr108,550,0249,115,571

    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)
    nssv18194369<0.001139296
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