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nsv6899734

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,986

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 114 SVs from 25 studies. See in: genome view    
    Submitted genomic65,635,268-65,640,253Question Mark
    Overlapping variant regions from other studies: 114 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):65,402,739-65,407,724Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6899734Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1165,635,26865,640,253
    nsv6899734RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1165,402,73965,407,724

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18585544duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18585544Submitted genomicNC_000011.10:g.656
    35268_65640253dup
    GRCh38 (hg38)NC_000011.10Chr1165,635,26865,640,253
    nssv18585544RemappedPerfectNC_000011.9:g.6540
    2739_65407724dup
    GRCh37.p13First PassNC_000011.9Chr1165,402,73965,407,724

    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)
    nssv185855441.8e-055275312
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