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nsv7043260

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,764,050

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8559 SVs from 111 studies. See in: genome view    
    Submitted genomic107,500,793-111,264,842Question Mark
    Overlapping variant regions from other studies: 8560 SVs from 111 studies. See in: genome view    
    Remapped(Score: Perfect):107,821,997-111,586,045Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7043260Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6107,500,793111,264,842
    nsv7043260RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6107,821,997111,586,045

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18777809inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18777809Submitted genomicNC_000006.12:g.107
    500793_111264842in
    v
    GRCh38 (hg38)NC_000006.12Chr6107,500,793111,264,842
    nssv18777809RemappedPerfectNC_000006.11:g.107
    821997_111586045in
    v
    GRCh37.p13First PassNC_000006.11Chr6107,821,997111,586,045

    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)
    nssv187778094e-061276268
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