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nsv7053023

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:262,565

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1317 SVs from 91 studies. See in: genome view    
    Submitted genomic212,286,605-212,549,169Question Mark
    Overlapping variant regions from other studies: 1317 SVs from 91 studies. See in: genome view    
    Remapped(Score: Perfect):213,151,330-213,413,893Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7053023Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2212,286,605212,549,169
    nsv7053023RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2213,151,330213,413,893

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767330inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767330Submitted genomicNC_000002.12:g.212
    286605_212549169in
    v
    GRCh38 (hg38)NC_000002.12Chr2212,286,605212,549,169
    nssv18767330RemappedPerfectNC_000002.11:g.213
    151330_213413893in
    v
    GRCh37.p13First PassNC_000002.11Chr2213,151,330213,413,893

    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)
    nssv187673304e-061276268
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