A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989190



Internal ID12971768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:97835738..97906802hg38UCSC Ensembl
Innerchr11:97706738..97777802hg19UCSC Ensembl
Innerchr11:97211948..97283012hg18UCSC Ensembl
Innerchr11:97211948..97283012hg17UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3871065
hg1971065
hg1871065
hg1771065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751038
Supporting Variants
SamplesBEC_101
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989190
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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