A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563845



Internal ID16351254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20216118..20244163hg38UCSC Ensembl
Innerchr14:20684277..20712322hg19UCSC Ensembl
Innerchr14:19754117..19782162hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3828046
hg1928046
hg1828046
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv823015
Samples
Known GenesOR11H4, OR11H6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563845
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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