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nsv4166466

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:147,311

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 198 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):33,495,757-33,643,067Question Mark
Overlapping variant regions from other studies: 198 SVs from 15 studies. See in: genome view    
Submitted genomic33,353,275-33,500,585Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4166466RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr833,495,75733,643,067
nsv4166466Submitted genomicGRCh37.p13Primary AssemblyNC_000008.10Chr833,353,27533,500,585

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15984120duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15984120RemappedPerfectNC_000008.11:g.334
95757_33643067dup
GRCh38.p12First PassNC_000008.11Chr833,495,75733,643,067
nssv15984120Submitted genomicNC_000008.10:g.333
53275_33500585dup
GRCh37.p13NC_000008.10Chr833,353,27533,500,585

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)
nssv159841204.6e-005121694
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