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nsv4320793

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:30,882

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 66 SVs from 10 studies. See in: genome view    
Remapped(Score: Perfect):133,941,717-133,972,598Question Mark
Overlapping variant regions from other studies: 66 SVs from 10 studies. See in: genome view    
Submitted genomic134,862,872-134,893,753Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4320793RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr4133,941,717133,972,598
nsv4320793Submitted genomicGRCh37.p13Primary AssemblyNC_000004.11Chr4134,862,872134,893,753

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16091330inversionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16091330RemappedPerfectNC_000004.12:g.133
941717_133972598in
v
GRCh38.p12First PassNC_000004.12Chr4133,941,717133,972,598
nssv16091330Submitted genomicNC_000004.11:g.134
862872_134893753in
v
GRCh37.p13NC_000004.11Chr4134,862,872134,893,753

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)
nssv160913304.6e-005121694
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