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nsv7044798

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:488,040

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1097 SVs from 65 studies. See in: genome view    
    Submitted genomic148,602,726-149,090,765Question Mark
    Overlapping variant regions from other studies: 1103 SVs from 66 studies. See in: genome view    
    Remapped(Score: Pass):149,360,295-149,947,279Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044798Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2148,602,726149,090,765
    nsv7044798RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2149,360,295149,947,279

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765927inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765927Submitted genomicNC_000002.12:g.148
    602726_149090765in
    v
    GRCh38 (hg38)NC_000002.12Chr2148,602,726149,090,765
    nssv18765927RemappedPassNC_000002.11:g.149
    360295_149947279in
    v
    GRCh37.p13First PassNC_000002.11Chr2149,360,295149,947,279

    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)
    nssv187659274e-061276268
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