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nsv6717253

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,591

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 90 SVs from 21 studies. See in: genome view    
    Submitted genomic32,387,103-32,394,693Question Mark
    Overlapping variant regions from other studies: 90 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):32,428,595-32,436,185Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6717253Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr332,387,10332,394,693
    nsv6717253RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr332,428,59532,436,185

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18678179duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18678179Submitted genomicNC_000003.12:g.323
    87103_32394693dup
    GRCh38 (hg38)NC_000003.12Chr332,387,10332,394,693
    nssv18678179RemappedPerfectNC_000003.11:g.324
    28595_32436185dup
    GRCh37.p13First PassNC_000003.11Chr332,428,59532,436,185

    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)
    nssv186781794e-061274174
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