A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563797



Internal ID16351206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19802472..19955745hg38UCSC Ensembl
Innerchr14:20270631..20423904hg19UCSC Ensembl
Innerchr14:19340471..19493744hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38153274
hg19153274
hg18153274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3527n54
Supporting Variantsnssv821690
Samples
Known GenesOR4K1, OR4K2, OR4K5, OR4N2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563797
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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