A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978815



Internal ID12979172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:48408848..48723513hg38UCSC Ensembl
Innerchr11:48430400..48745065hg19UCSC Ensembl
Innerchr11:48386976..48701641hg18UCSC Ensembl
Innerchr11:48386976..48701641hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38314666
hg19314666
hg18314666
hg17314666
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34253
Supporting Variants
SamplesNA12716
Known GenesOR4A47
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978815
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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