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nsv7038554

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:212,126

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 635 SVs from 67 studies. See in: genome view    
    Submitted genomic236,483,618-236,695,743Question Mark
    Overlapping variant regions from other studies: 635 SVs from 67 studies. See in: genome view    
    Remapped(Score: Perfect):237,392,261-237,604,386Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7038554Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2236,483,618236,695,743
    nsv7038554RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2237,392,261237,604,386

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767802inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767802Submitted genomicNC_000002.12:g.236
    483618_236695743in
    v
    GRCh38 (hg38)NC_000002.12Chr2236,483,618236,695,743
    nssv18767802RemappedPerfectNC_000002.11:g.237
    392261_237604386in
    v
    GRCh37.p13First PassNC_000002.11Chr2237,392,261237,604,386

    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)
    nssv187678024e-061276268
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