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nsv6547492

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:367

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 164 SVs from 22 studies. See in: genome view    
    Submitted genomic173,819,346-173,819,712Question Mark
    Overlapping variant regions from other studies: 167 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):173,788,484-173,788,850Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6547492Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1173,819,346173,819,712
    nsv6547492RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1173,788,484173,788,850

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18248699inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18248699Submitted genomicNC_000001.11:g.173
    819346_173819712in
    v
    GRCh38 (hg38)NC_000001.11Chr1173,819,346173,819,712
    nssv18248699RemappedPerfectNC_000001.10:g.173
    788484_173788850in
    v
    GRCh37.p13First PassNC_000001.10Chr1173,788,484173,788,850

    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)
    nssv18248699<0.001336640
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