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nsv6648045

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:738,900

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2213 SVs from 83 studies. See in: genome view    
    Submitted genomic26,400,001-27,138,900Question Mark
    Overlapping variant regions from other studies: 2214 SVs from 83 studies. See in: genome view    
    Remapped(Score: Perfect):26,726,492-27,465,391Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6648045Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr126,400,00127,138,900
    nsv6648045RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr126,726,49227,465,391

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18610390duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18610390Submitted genomicNC_000001.11:g.264
    00001_27138900dup
    GRCh38 (hg38)NC_000001.11Chr126,400,00127,138,900
    nssv18610390RemappedPerfectNC_000001.10:g.267
    26492_27465391dup
    GRCh37.p13First PassNC_000001.10Chr126,726,49227,465,391

    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)
    nssv186103904e-061248922
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