A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989289



Internal ID12626615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2170634..2836432hg38UCSC Ensembl
Innerchr3:2212318..2878116hg19UCSC Ensembl
Innerchr3:2187318..2853116hg18UCSC Ensembl
Innerchr3:2187318..2853116hg17UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38665799
hg19665799
hg18665799
hg17665799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751993
Supporting Variants
SamplesBEC_40
Known GenesCNTN4
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989289
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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