A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152435



Internal ID15529600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1808863..2199963hg38UCSC Ensembl
Innerchr3:1850547..2241647hg19UCSC Ensembl
Innerchr3:1825547..2216647hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38391101
hg19391101
hg18391101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589362
Supporting Variants
SamplesHGDP00815
Known GenesCNTN4, CNTN4-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152435
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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