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nsv7043423

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:50

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 99 SVs from 22 studies. See in: genome view    
    Submitted genomic49,733,069-49,733,118Question Mark
    Overlapping variant regions from other studies: 99 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):49,700,782-49,700,831Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7043423Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr649,733,06949,733,118
    nsv7043423RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr649,700,78249,700,831

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18778143inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18778143Submitted genomicNC_000006.12:g.497
    33069_49733118inv
    GRCh38 (hg38)NC_000006.12Chr649,733,06949,733,118
    nssv18778143RemappedPerfectNC_000006.11:g.497
    00782_49700831inv
    GRCh37.p13First PassNC_000006.11Chr649,700,78249,700,831

    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)
    nssv18778143<0.001213273448
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