A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985902



Internal ID12637543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31115277..31274377hg38UCSC Ensembl
Innerchr11:31136824..31295924hg19UCSC Ensembl
Innerchr11:31093400..31252500hg18UCSC Ensembl
Innerchr11:31093400..31252500hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38159101
hg19159101
hg18159101
hg17159101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751022
Supporting Variants
SamplesSPC_83
Known GenesDCDC1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985902
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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