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nsv7029237

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:237,968

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1242 SVs from 86 studies. See in: genome view    
    Submitted genomic62,545,258-62,783,225Question Mark
    Overlapping variant regions from other studies: 913 SVs from 83 studies. See in: genome view    
    Remapped(Score: Pass):61,267,734-61,414,577Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7029237Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2062,545,25862,783,225
    nsv7029237RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2061,267,73461,414,577

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18645981duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18645981Submitted genomicNC_000020.11:g.625
    45258_62783225dup
    GRCh38 (hg38)NC_000020.11Chr2062,545,25862,783,225
    nssv18645981RemappedPassNC_000020.10:g.612
    67734_61414577dup
    GRCh37.p13First PassNC_000020.10Chr2061,267,73461,414,577

    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)
    nssv186459814e-061275822
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