A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751038



Internal ID12984590
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 StatusM
Merged Variants
Supporting Variantsessv6989190, essv6980653
SamplesBEC_101
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2751038
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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