A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981020



Internal ID12625991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2731887..2838610hg38UCSC Ensembl
Innerchr3:2773571..2880294hg19UCSC Ensembl
Innerchr3:2748571..2855294hg18UCSC Ensembl
Innerchr3:2748571..2855294hg17UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38106724
hg19106724
hg18106724
hg17106724
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751998
Supporting Variants
SamplesBEC_337
Known GenesCNTN4
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981020
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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