A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892118



Internal ID19186514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134483933..134851958hg38UCSC Ensembl
Outerchr11:134424836..134869255hg38UCSC Ensembl
Innerchr11:134353827..134721852hg19UCSC Ensembl
Outerchr11:134294730..134739149hg19UCSC Ensembl
Innerchr11:133859037..134227062hg18UCSC Ensembl
Outerchr11:133799940..134244359hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38444420
hg19444420
hg18444420
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790032, essv25790434
Samples
Known GenesLOC283177
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892118
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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