nsv6554514

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:978

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 188 SVs from 26 studies. See in: genome view    
    Submitted genomic165,338,265-165,339,242Question Mark
    Overlapping variant regions from other studies: 188 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):166,194,775-166,195,752Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6554514Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2165,338,265165,339,242
    nsv6554514RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2166,194,775166,195,752

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18255828inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18255828Submitted genomicNC_000002.12:g.165
    338265_165339242in
    v
    GRCh38 (hg38)NC_000002.12Chr2165,338,265165,339,242
    nssv18255828RemappedPerfectNC_000002.11:g.166
    194775_166195752in
    v
    GRCh37.p13First PassNC_000002.11Chr2166,194,775166,195,752

    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)
    nssv18255828<0.001237290
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