A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985114



Internal ID12982797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134506896..134846896hg38UCSC Ensembl
Innerchr11:134376790..134716790hg19UCSC Ensembl
Innerchr11:133882000..134222000hg18UCSC Ensembl
Innerchr11:133882000..134222000hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38340001
hg19340001
hg18340001
hg17340001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750986
Supporting Variants
SamplesSPC_10
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985114
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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