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nsv6549702

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:972

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 121 SVs from 18 studies. See in: genome view    
    Submitted genomic205,726,029-205,727,000Question Mark
    Overlapping variant regions from other studies: 121 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):205,695,157-205,696,128Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6549702Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1205,726,029205,727,000
    nsv6549702RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1205,695,157205,696,128

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18249984inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18249984Submitted genomicNC_000001.11:g.205
    726029_205727000in
    v
    GRCh38 (hg38)NC_000001.11Chr1205,726,029205,727,000
    nssv18249984RemappedPerfectNC_000001.10:g.205
    695157_205696128in
    v
    GRCh37.p13First PassNC_000001.10Chr1205,695,157205,696,128

    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)
    nssv18249984<0.001136136
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