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nsv7061741

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,631,120

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 12198 SVs from 117 studies. See in: genome view    
    Submitted genomic100,793,881-105,425,000Question Mark
    Overlapping variant regions from other studies: 12198 SVs from 117 studies. See in: genome view    
    Remapped(Score: Perfect):100,664,612-105,295,727Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7061741Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11100,793,881105,425,000
    nsv7061741RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11100,664,612105,295,727

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18737505inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18737505Submitted genomicNC_000011.10:g.100
    793881_105425000in
    v
    GRCh38 (hg38)NC_000011.10Chr11100,793,881105,425,000
    nssv18737505RemappedPerfectNC_000011.9:g.1006
    64612_105295727inv
    GRCh37.p13First PassNC_000011.9Chr11100,664,612105,295,727

    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)
    nssv187375054e-061276268
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