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nsv6513850

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:279,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1072 SVs from 82 studies. See in: genome view    
    Submitted genomic36,351,001-36,630,200Question Mark
    Overlapping variant regions from other studies: 635 SVs from 47 studies. See in: genome view    
    Remapped(Score: Pass):235,757-429,138Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6513850Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1736,351,00136,630,200
    nsv6513850RemappedPassGRCh37.p13PATCHESFirst PassNW_003315949.1Chr17|NW_0
    03315949.1
    235,757429,138

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18182089duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18182089Submitted genomicNC_000017.11:g.363
    51001_36630200dup
    GRCh38 (hg38)NC_000017.11Chr1736,351,00136,630,200
    nssv18182089RemappedPassNW_003315949.1:g.2
    35757_429138dup
    GRCh37.p13First PassNW_003315949.1Chr17|NW_0
    03315949.1
    235,757429,138

    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)
    nssv18182089<0.001235492
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