A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798177



Internal ID18813075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4268493..4355975hg38UCSC Ensembl
Innerchr11:4289723..4377205hg19UCSC Ensembl
Innerchr11:4246299..4333781hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3887483
hg1987483
hg1887483
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891912
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798177
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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