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nsv6552383

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:495

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 125 SVs from 21 studies. See in: genome view    
    Submitted genomic135,834,929-135,835,423Question Mark
    Overlapping variant regions from other studies: 125 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):136,592,499-136,592,993Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6552383Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2135,834,929135,835,423
    nsv6552383RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2136,592,499136,592,993

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18255917inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18255917Submitted genomicNC_000002.12:g.135
    834929_135835423in
    v
    GRCh38 (hg38)NC_000002.12Chr2135,834,929135,835,423
    nssv18255917RemappedPerfectNC_000002.11:g.136
    592499_136592993in
    v
    GRCh37.p13First PassNC_000002.11Chr2136,592,499136,592,993

    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)
    nssv18255917<0.001538582
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