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nsv6605214

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:851,726

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3220 SVs from 100 studies. See in: genome view    
    Submitted genomic101,291,401-102,143,126Question Mark
    Overlapping variant regions from other studies: 2934 SVs from 99 studies. See in: genome view    
    Remapped(Score: Pass):100,934,682-101,718,950Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6605214Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7101,291,401102,143,126
    nsv6605214RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7100,934,682101,718,950

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18234664duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18234664Submitted genomicNC_000007.14:g.101
    291401_102143126du
    p
    GRCh38 (hg38)NC_000007.14Chr7101,291,401102,143,126
    nssv18234664RemappedPassNC_000007.13:g.100
    934682_101718950du
    p
    GRCh37.p13First PassNC_000007.13Chr7100,934,682101,718,950

    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)
    nssv18234664<0.001139272
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