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nsv6538139

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:396

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 165 SVs from 23 studies. See in: genome view    
    Submitted genomic173,801,982-173,802,377Question Mark
    Overlapping variant regions from other studies: 168 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):173,771,120-173,771,515Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6538139Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1173,801,982173,802,377
    nsv6538139RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1173,771,120173,771,515

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18248698inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18248698Submitted genomicNC_000001.11:g.173
    801982_173802377in
    v
    GRCh38 (hg38)NC_000001.11Chr1173,801,982173,802,377
    nssv18248698RemappedPerfectNC_000001.10:g.173
    771120_173771515in
    v
    GRCh37.p13First PassNC_000001.10Chr1173,771,120173,771,515

    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)
    nssv18248698<0.001136320
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