A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892077



Internal ID19186473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96508137..96516160hg38UCSC Ensembl
Outerchr11:96508137..96516160hg38UCSC Ensembl
Innerchr11:96241301..96249324hg19UCSC Ensembl
Outerchr11:96241301..96249324hg19UCSC Ensembl
Innerchr11:95880949..95888972hg18UCSC Ensembl
Outerchr11:95880949..95888972hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg388024
hg198024
hg188024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797824
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892077
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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