A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985113



Internal ID12982796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134492244..134846515hg38UCSC Ensembl
Innerchr11:134362138..134716409hg19UCSC Ensembl
Innerchr11:133867348..134221619hg18UCSC Ensembl
Innerchr11:133867348..134221619hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38354272
hg19354272
hg18354272
hg17354272
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750986
Supporting Variants
SamplesSPC_10
Known GenesLOC283177
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985113
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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