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nsv6536769

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:806,031

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1274 SVs from 73 studies. See in: genome view    
    Submitted genomic144,077,918-144,883,948Question Mark
    Overlapping variant regions from other studies: 1510 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):893,331-1,699,361Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6536769Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1144,077,918144,883,948
    nsv6536769RemappedPerfectGRCh37.p13PATCHESFirst PassNW_003871055.3Chr1|NW_00
    3871055.3
    893,3311,699,361

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18247025inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18247025Submitted genomicNC_000001.11:g.144
    077918_144883948in
    v
    GRCh38 (hg38)NC_000001.11Chr1144,077,918144,883,948
    nssv18247025RemappedPerfectNW_003871055.3:g.8
    93331_1699361inv
    GRCh37.p13First PassNW_003871055.3Chr1|NW_00
    3871055.3
    893,3311,699,361

    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)
    nssv18247025<0.0011238600
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