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nsv6912721

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:105

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 69 SVs from 20 studies. See in: genome view    
    Submitted genomic61,782,988-61,783,092Question Mark
    Overlapping variant regions from other studies: 69 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):61,550,460-61,550,564Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6912721Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1161,782,98861,783,092
    nsv6912721RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1161,550,46061,550,564

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18585372duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18585372Submitted genomicNC_000011.10:g.617
    82988_61783092dup
    GRCh38 (hg38)NC_000011.10Chr1161,782,98861,783,092
    nssv18585372RemappedPerfectNC_000011.9:g.6155
    0460_61550564dup
    GRCh37.p13First PassNC_000011.9Chr1161,550,46061,550,564

    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)
    nssv185853724e-061227152
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