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nsv6881795

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:28,622

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 193 SVs from 34 studies. See in: genome view    
    Submitted genomic114,863,438-114,892,059Question Mark
    Overlapping variant regions from other studies: 193 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):116,623,197-116,651,818Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6881795Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr10114,863,438114,892,059
    nsv6881795RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr10116,623,197116,651,818

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18585852duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18585852Submitted genomicNC_000010.11:g.114
    863438_114892059du
    p
    GRCh38 (hg38)NC_000010.11Chr10114,863,438114,892,059
    nssv18585852RemappedPerfectNC_000010.10:g.116
    623197_116651818du
    p
    GRCh37.p13First PassNC_000010.10Chr10116,623,197116,651,818

    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)
    nssv185858525.7e-0516275638
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