A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985112



Internal ID12982790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134478027..134860776hg38UCSC Ensembl
Innerchr11:134347921..134730670hg19UCSC Ensembl
Innerchr11:133853131..134235880hg18UCSC Ensembl
Innerchr11:133853131..134235880hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38382750
hg19382750
hg18382750
hg17382750
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)essv6985112
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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