A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563778



Internal ID16351187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19745778..19958583hg38UCSC Ensembl
Innerchr14:20213937..20426742hg19UCSC Ensembl
Innerchr14:19283777..19496582hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38212806
hg19212806
hg18212806
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3520n54
Supporting Variantsnssv821665
Samples
Known GenesOR4K1, 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)nsv563778
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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