A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790434



Internal ID19169026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134483933..134851958hg38UCSC Ensembl
Innerchr11:134353827..134721852hg19UCSC Ensembl
Innerchr11:133859037..134227062hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38368026
hg19368026
hg18368026
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892118
Supporting Variants
Samples
Known GenesLOC283177
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=151
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790434
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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