A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751021



Internal ID12984573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25440265..25565110hg38UCSC Ensembl
Innerchr11:25461811..25586656hg19UCSC Ensembl
Innerchr11:25418387..25543232hg18UCSC Ensembl
Innerchr11:25418387..25543232hg17UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38124846
hg19124846
hg18124846
hg17124846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6983231, essv6989760, essv6983232
SamplesBEC_558
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)esv2751021
Frequency
Sample Size771
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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