A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3711188



Internal ID19009469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19637241..19924615hg38UCSC Ensembl
Innerchr14:20105479..20392774hg19UCSC Ensembl
Innerchr14:19175240..19462614hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38287375
hg19287296
hg18287375
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037249
Supporting Variants
Samples
Known GenesOR11H2, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3711188
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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