A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986918



Internal ID12633813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2232536..2446016hg38UCSC Ensembl
Innerchr3:2274220..2487700hg19UCSC Ensembl
Innerchr3:2249220..2462700hg18UCSC Ensembl
Innerchr3:2249220..2462700hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38213481
hg19213481
hg18213481
hg17213481
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34352
Supporting Variants
SamplesNA18592
Known GenesCNTN4
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986918
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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