A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148558



Internal ID15533990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:21605322..21836913hg38UCSC Ensembl
Innerchr14:22073473..22305071hg19UCSC Ensembl
Innerchr14:21143313..21374911hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38231592
hg19231599
hg18231599
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv563851
Supporting Variants
SamplesNINDS_244
Known GenesOR10G2, OR4E2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148558
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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