A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv821696



Internal ID16115652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19837272..19956348hg38UCSC Ensembl
Innerchr14:20305431..20424507hg19UCSC Ensembl
Innerchr14:19375271..19494347hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38119077
hg19119077
hg18119077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563803
Supporting Variants
Samples
Known GenesOR4K1, OR4K2, OR4K5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv821696
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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