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nsv5506177

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,309

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 104 SVs from 29 studies. See in: genome view    
Submitted genomic118,380,326-118,382,634Question Mark
Overlapping variant regions from other studies: 104 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):118,818,131-118,820,439Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5506177Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12118,380,326118,382,634
nsv5506177RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12118,818,131118,820,439

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17684799deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17684799Submitted genomicNC_000012.12:g.118
380326_118382634de
l
GRCh38 (hg38)NC_000012.12Chr12118,380,326118,382,634
nssv17684799RemappedPerfectNC_000012.11:g.118
818131_118820439de
l
GRCh37.p13First PassNC_000012.11Chr12118,818,131118,820,439

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)
nssv17684799<0.00116404
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