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nsv6568046

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:939

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 104 SVs from 18 studies. See in: genome view    
    Submitted genomic157,595,985-157,596,923Question Mark
    Overlapping variant regions from other studies: 104 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):157,313,774-157,314,712Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6568046Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3157,595,985157,596,923
    nsv6568046RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3157,313,774157,314,712

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18261051inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18261051Submitted genomicNC_000003.12:g.157
    595985_157596923in
    v
    GRCh38 (hg38)NC_000003.12Chr3157,595,985157,596,923
    nssv18261051RemappedPerfectNC_000003.11:g.157
    313774_157314712in
    v
    GRCh37.p13First PassNC_000003.11Chr3157,313,774157,314,712

    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)
    nssv18261051<0.001233394
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