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nsv7015435

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,222,501

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3804 SVs from 97 studies. See in: genome view    
    Submitted genomic4,445,183-5,667,683Question Mark
    Overlapping variant regions from other studies: 3805 SVs from 97 studies. See in: genome view    
    Remapped(Score: Perfect):4,425,830-5,648,329Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7015435Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr204,445,1835,667,683
    nsv7015435RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr204,425,8305,648,329

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18642140duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18642140Submitted genomicNC_000020.11:g.444
    5183_5667683dup
    GRCh38 (hg38)NC_000020.11Chr204,445,1835,667,683
    nssv18642140RemappedPerfectNC_000020.10:g.442
    5830_5648329dup
    GRCh37.p13First PassNC_000020.10Chr204,425,8305,648,329

    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)
    nssv186421404e-061275520
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