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nsv7047005

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:33

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 128 SVs from 23 studies. See in: genome view    
    Submitted genomic192,862,701-192,862,733Question Mark
    Overlapping variant regions from other studies: 128 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):192,580,490-192,580,522Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7047005Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3192,862,701192,862,733
    nsv7047005RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3192,580,490192,580,522

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18770918inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18770918Submitted genomicNC_000003.12:g.192
    862701_192862733in
    v
    GRCh38 (hg38)NC_000003.12Chr3192,862,701192,862,733
    nssv18770918RemappedPerfectNC_000003.11:g.192
    580490_192580522in
    v
    GRCh37.p13First PassNC_000003.11Chr3192,580,490192,580,522

    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)
    nssv187709184e-061276268
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