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nsv6846158

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,063,500

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 2879 SVs from 92 studies. See in: genome view    
    Submitted genomic19,219,901-20,283,400Question Mark
    Overlapping variant regions from other studies: 2881 SVs from 92 studies. See in: genome view    
    Remapped(Score: Perfect):19,077,411-20,140,911Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6846158Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr819,219,90120,283,400
    nsv6846158RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr819,077,41120,140,911

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18736640duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18736640Submitted genomicNC_000008.11:g.192
    19901_20283400dup
    GRCh38 (hg38)NC_000008.11Chr819,219,90120,283,400
    nssv18736640RemappedPerfectNC_000008.10:g.190
    77411_20140911dup
    GRCh37.p13First PassNC_000008.10Chr819,077,41120,140,911

    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)
    nssv187366404e-061274908
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