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nsv7067435

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:33,214

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 767 SVs from 73 studies. See in: genome view    
    Submitted genomic1,244,682-1,277,895Question Mark
    Overlapping variant regions from other studies: 767 SVs from 73 studies. See in: genome view    
    Remapped(Score: Perfect):1,294,683-1,327,896Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7067435Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr161,244,6821,277,895
    nsv7067435RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr161,294,6831,327,896

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756835inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756835Submitted genomicNC_000016.10:g.124
    4682_1277895inv
    GRCh38 (hg38)NC_000016.10Chr161,244,6821,277,895
    nssv18756835RemappedPerfectNC_000016.9:g.1294
    683_1327896inv
    GRCh37.p13First PassNC_000016.9Chr161,294,6831,327,896

    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)
    nssv187568354e-061276268
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