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nsv6942786

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:224,422

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 653 SVs from 48 studies. See in: genome view    
    Submitted genomic95,402,632-95,627,053Question Mark
    Overlapping variant regions from other studies: 653 SVs from 48 studies. See in: genome view    
    Remapped(Score: Perfect):96,054,886-96,279,307Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6942786Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1395,402,63295,627,053
    nsv6942786RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1396,054,88696,279,307

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18611448duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18611448Submitted genomicNC_000013.11:g.954
    02632_95627053dup
    GRCh38 (hg38)NC_000013.11Chr1395,402,63295,627,053
    nssv18611448RemappedPerfectNC_000013.10:g.960
    54886_96279307dup
    GRCh37.p13First PassNC_000013.10Chr1396,054,88696,279,307

    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)
    nssv186114481.1e-053275224
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