A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788627



Internal ID19162707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:95317959..95583117hg38UCSC Ensembl
Innerchr11:95051123..95316281hg19UCSC Ensembl
Innerchr11:94690771..94955929hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38265159
hg19265159
hg18265159
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892076
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=93
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788627
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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