A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037192



Internal ID19126411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19851530..19945687hg38UCSC Ensembl
Innerchr14:20319689..20413846hg19UCSC Ensembl
Innerchr14:19389529..19483686hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3894158
hg1994158
hg1894158
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1789n100
Supporting Variantsnssv3712118
Samples
Known GenesOR4K1, OR4K2, OR4K5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037192
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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