A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv821519



Internal ID16115475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19616004..19969990hg38UCSC Ensembl
Innerchr14:20084006..20438149hg19UCSC Ensembl
Innerchr14:19154003..19507989hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38353987
hg19354144
hg18353987
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563742
Supporting Variants
Samples
Known GenesOR11H2, OR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv821519
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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