A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527384



Internal ID18825665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19350746..19952068hg38UCSC Ensembl
Innerchr14:19938429..20420227hg19UCSC Ensembl
Innerchr14:19008429..19490067hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38601323
hg19481799
hg18481639
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040157
Supporting Variants
Samples
Known GenesOR11H2, OR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3, POTEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3527384
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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