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nsv5498435

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:537

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 81 SVs from 21 studies. See in: genome view    
Submitted genomic108,782,601-108,783,137Question Mark
Overlapping variant regions from other studies: 81 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):109,176,377-109,176,913Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5498435Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12108,782,601108,783,137
nsv5498435RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12109,176,377109,176,913

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17684330duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17684330Submitted genomicNC_000012.12:g.108
782601_108783137du
p
GRCh38 (hg38)NC_000012.12Chr12108,782,601108,783,137
nssv17684330RemappedPerfectNC_000012.11:g.109
176377_109176913du
p
GRCh37.p13First PassNC_000012.11Chr12109,176,377109,176,913

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)
nssv17684330<0.00116404
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