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nsv7039900

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:78

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 106 SVs from 19 studies. See in: genome view    
    Submitted genomic210,140,325-210,140,402Question Mark
    Overlapping variant regions from other studies: 106 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):211,005,049-211,005,126Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7039900Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2210,140,325210,140,402
    nsv7039900RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2211,005,049211,005,126

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767656inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767656Submitted genomicNC_000002.12:g.210
    140325_210140402in
    v
    GRCh38 (hg38)NC_000002.12Chr2210,140,325210,140,402
    nssv18767656RemappedPerfectNC_000002.11:g.211
    005049_211005126in
    v
    GRCh37.p13First PassNC_000002.11Chr2211,005,049211,005,126

    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)
    nssv187676567.5e-0520274116
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