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nsv7044524

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:223,324

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 745 SVs from 64 studies. See in: genome view    
    Submitted genomic231,260,277-231,483,600Question Mark
    Overlapping variant regions from other studies: 745 SVs from 64 studies. See in: genome view    
    Remapped(Score: Good):232,124,990-232,348,311Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044524Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2231,260,277231,483,600
    nsv7044524RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2232,124,990232,348,311

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18767720inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18767720Submitted genomicNC_000002.12:g.231
    260277_231483600in
    v
    GRCh38 (hg38)NC_000002.12Chr2231,260,277231,483,600
    nssv18767720RemappedGoodNC_000002.11:g.232
    124990_232348311in
    v
    GRCh37.p13First PassNC_000002.11Chr2232,124,990232,348,311

    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)
    nssv187677204e-061276268
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