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nsv6714902

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:94

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 58 SVs from 15 studies. See in: genome view    
    Submitted genomic23,948,461-23,948,554Question Mark
    Overlapping variant regions from other studies: 58 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):23,989,952-23,990,045Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6714902Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr323,948,46123,948,554
    nsv6714902RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr323,989,95223,990,045

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18677490duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18677490Submitted genomicNC_000003.12:g.239
    48461_23948554dup
    GRCh38 (hg38)NC_000003.12Chr323,948,46123,948,554
    nssv18677490RemappedPerfectNC_000003.11:g.239
    89952_23990045dup
    GRCh37.p13First PassNC_000003.11Chr323,989,95223,990,045

    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)
    nssv18677490<0.00132225278
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