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nsv7048636

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:200,331

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 582 SVs from 50 studies. See in: genome view    
    Submitted genomic138,740,942-138,941,272Question Mark
    Overlapping variant regions from other studies: 582 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):139,062,079-139,262,409Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7048636Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6138,740,942138,941,272
    nsv7048636RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6139,062,079139,262,409

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18780223inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18780223Submitted genomicNC_000006.12:g.138
    740942_138941272in
    v
    GRCh38 (hg38)NC_000006.12Chr6138,740,942138,941,272
    nssv18780223RemappedPerfectNC_000006.11:g.139
    062079_139262409in
    v
    GRCh37.p13First PassNC_000006.11Chr6139,062,079139,262,409

    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)
    nssv187802237e-062274930
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