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nsv6941112

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:261,520

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 583 SVs from 56 studies. See in: genome view    
    Submitted genomic95,516,361-95,777,880Question Mark
    Overlapping variant regions from other studies: 583 SVs from 56 studies. See in: genome view    
    Remapped(Score: Perfect):96,168,615-96,430,134Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6941112Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1395,516,36195,777,880
    nsv6941112RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1396,168,61596,430,134

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18611456duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18611456Submitted genomicNC_000013.11:g.955
    16361_95777880dup
    GRCh38 (hg38)NC_000013.11Chr1395,516,36195,777,880
    nssv18611456RemappedPerfectNC_000013.10:g.961
    68615_96430134dup
    GRCh37.p13First PassNC_000013.10Chr1396,168,61596,430,134

    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)
    nssv186114561.1e-053275074
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