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nsv6550079

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:469

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 185 SVs from 29 studies. See in: genome view    
    Submitted genomic173,954,945-173,955,413Question Mark
    Overlapping variant regions from other studies: 188 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):173,924,083-173,924,551Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6550079Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1173,954,945173,955,413
    nsv6550079RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1173,924,083173,924,551

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18248715inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18248715Submitted genomicNC_000001.11:g.173
    954945_173955413in
    v
    GRCh38 (hg38)NC_000001.11Chr1173,954,945173,955,413
    nssv18248715RemappedPerfectNC_000001.10:g.173
    924083_173924551in
    v
    GRCh37.p13First PassNC_000001.10Chr1173,924,083173,924,551

    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)
    nssv18248715<0.001534480
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