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nsv7041072

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:483,872

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1087 SVs from 65 studies. See in: genome view    
    Submitted genomic148,602,723-149,086,594Question Mark
    Overlapping variant regions from other studies: 1093 SVs from 66 studies. See in: genome view    
    Remapped(Score: Pass):149,360,292-149,943,108Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7041072Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2148,602,723149,086,594
    nsv7041072RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2149,360,292149,943,108

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18765926inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18765926Submitted genomicNC_000002.12:g.148
    602723_149086594in
    v
    GRCh38 (hg38)NC_000002.12Chr2148,602,723149,086,594
    nssv18765926RemappedPassNC_000002.11:g.149
    360292_149943108in
    v
    GRCh37.p13First PassNC_000002.11Chr2149,360,292149,943,108

    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)
    nssv187659264e-061276268
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