nsv6608026

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:869,269

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3623 SVs from 92 studies. See in: genome view    
    Submitted genomic169,180,752-170,050,020Question Mark
    Overlapping variant regions from other studies: 3177 SVs from 92 studies. See in: genome view    
    Remapped(Score: Pass):169,580,847-170,365,244Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6608026Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6169,180,752170,050,020
    nsv6608026RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6169,580,847170,365,244

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18139912deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18139912Submitted genomicNC_000006.12:g.169
    180752_170050020de
    l
    GRCh38 (hg38)NC_000006.12Chr6169,180,752170,050,020
    nssv18139912RemappedPassNC_000006.11:g.169
    580847_170365244de
    l
    GRCh37.p13First PassNC_000006.11Chr6169,580,847170,365,244

    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)
    nssv18139912<0.001139230
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