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nsv6563993

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,190

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 95 SVs from 22 studies. See in: genome view    
    Submitted genomic183,880,868-183,882,057Question Mark
    Overlapping variant regions from other studies: 95 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):183,598,656-183,599,845Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6563993Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3183,880,868183,882,057
    nsv6563993RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3183,598,656183,599,845

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18260569inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18260569Submitted genomicNC_000003.12:g.183
    880868_183882057in
    v
    GRCh38 (hg38)NC_000003.12Chr3183,880,868183,882,057
    nssv18260569RemappedPerfectNC_000003.11:g.183
    598656_183599845in
    v
    GRCh37.p13First PassNC_000003.11Chr3183,598,656183,599,845

    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)
    nssv18260569<0.001136214
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