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nsv6401167

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,173

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 121 SVs from 24 studies. See in: genome view    
    Submitted genomic11,118,947-11,123,119Question Mark
    Overlapping variant regions from other studies: 121 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):11,119,180-11,123,352Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6401167Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr611,118,94711,123,119
    nsv6401167RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr611,119,18011,123,352

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18135397deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18135397Submitted genomicNC_000006.12:g.111
    18947_11123119del
    GRCh38 (hg38)NC_000006.12Chr611,118,94711,123,119
    nssv18135397RemappedPerfectNC_000006.11:g.111
    19180_11123352del
    GRCh37.p13First PassNC_000006.11Chr611,119,18011,123,352

    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)
    nssv18135397<0.001339218
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