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nsv6722833

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:165,009

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 904 SVs from 75 studies. See in: genome view    
    Submitted genomic40,004,765-40,169,773Question Mark
    Overlapping variant regions from other studies: 904 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):40,006,385-40,171,393Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6722833Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr440,004,76540,169,773
    nsv6722833RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr440,006,38540,171,393

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18688582duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18688582Submitted genomicNC_000004.12:g.400
    04765_40169773dup
    GRCh38 (hg38)NC_000004.12Chr440,004,76540,169,773
    nssv18688582RemappedPerfectNC_000004.11:g.400
    06385_40171393dup
    GRCh37.p13First PassNC_000004.11Chr440,006,38540,171,393

    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)
    nssv186885824e-061275792
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