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nsv7069281

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,464,145

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 13435 SVs from 106 studies. See in: genome view    
    Submitted genomic107,936,485-114,400,629Question Mark
    Overlapping variant regions from other studies: 13440 SVs from 106 studies. See in: genome view    
    Remapped(Score: Perfect):107,807,211-114,271,351Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7069281Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr11107,936,485114,400,629
    nsv7069281RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr11107,807,211114,271,351

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18749743inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18749743Submitted genomicNC_000011.10:g.107
    936485_114400629in
    v
    GRCh38 (hg38)NC_000011.10Chr11107,936,485114,400,629
    nssv18749743RemappedPerfectNC_000011.9:g.1078
    07211_114271351inv
    GRCh37.p13First PassNC_000011.9Chr11107,807,211114,271,351

    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)
    nssv187497434e-061276268
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