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nsv6538958

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:521

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 170 SVs from 41 studies. See in: genome view    
    Submitted genomic129,974,302-129,974,822Question Mark
    Overlapping variant regions from other studies: 170 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):130,731,875-130,732,395Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6538958Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2129,974,302129,974,822
    nsv6538958RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2130,731,875130,732,395

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18256834inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18256834Submitted genomicNC_000002.12:g.129
    974302_129974822in
    v
    GRCh38 (hg38)NC_000002.12Chr2129,974,302129,974,822
    nssv18256834RemappedPerfectNC_000002.11:g.130
    731875_130732395in
    v
    GRCh37.p13First PassNC_000002.11Chr2130,731,875130,732,395

    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)
    nssv18256834<0.001534840
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