A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979647



Internal ID12633819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2323936..2445596hg38UCSC Ensembl
Innerchr3:2365620..2487280hg19UCSC Ensembl
Innerchr3:2340620..2462280hg18UCSC Ensembl
Innerchr3:2340620..2462280hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38121661
hg19121661
hg18121661
hg17121661
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979647
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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