A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524093



Internal ID15451386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:21106531..21184738hg38UCSC Ensembl
Innerchr14:21574690..21652897hg19UCSC Ensembl
Innerchr14:20644530..20722737hg18UCSC Ensembl
Innerchr14:20644530..20722737hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3878208
hg1978208
hg1878208
hg1778208
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699966
Samples
Known GenesOR5AU1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524093
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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