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nsv6962700

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:149

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 74 SVs from 18 studies. See in: genome view    
    Submitted genomic92,572,127-92,572,275Question Mark
    Overlapping variant regions from other studies: 74 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):93,038,472-93,038,620Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6962700Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1492,572,12792,572,275
    nsv6962700RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1493,038,47293,038,620

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18615443duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18615443Submitted genomicNC_000014.9:g.9257
    2127_92572275dup
    GRCh38 (hg38)NC_000014.9Chr1492,572,12792,572,275
    nssv18615443RemappedPerfectNC_000014.8:g.9303
    8472_93038620dup
    GRCh37.p13First PassNC_000014.8Chr1493,038,47293,038,620

    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)
    nssv186154432.6e-056223860
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