A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790722



Internal ID19171765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54944514..55187440hg38UCSC Ensembl
Innerchr11:54711990..54954916hg19UCSC Ensembl
Innerchr11:54468566..54711492hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38242927
hg19242927
hg18242927
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892010
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=30
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790722
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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