A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527413



Internal ID18825694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19424960..19954424hg38UCSC Ensembl
Innerchr14:20010901..20422583hg19UCSC Ensembl
Innerchr14:19080901..19492423hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38529465
hg19411683
hg18411523
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042228
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)nssv3527413
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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