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nsv7053039

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,044,345

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3438 SVs from 96 studies. See in: genome view    
    Submitted genomic183,766,927-184,811,271Question Mark
    Overlapping variant regions from other studies: 3440 SVs from 96 studies. See in: genome view    
    Remapped(Score: Perfect):184,688,080-185,732,425Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7053039Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4183,766,927184,811,271
    nsv7053039RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4184,688,080185,732,425

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18773976inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18773976Submitted genomicNC_000004.12:g.183
    766927_184811271in
    v
    GRCh38 (hg38)NC_000004.12Chr4183,766,927184,811,271
    nssv18773976RemappedPerfectNC_000004.11:g.184
    688080_185732425in
    v
    GRCh37.p13First PassNC_000004.11Chr4184,688,080185,732,425

    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)
    nssv187739764e-061276268
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