A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782522



Internal ID19164666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:13061506..13094185hg38UCSC Ensembl
Innerchr11:13083053..13115732hg19UCSC Ensembl
Innerchr11:13039629..13072308hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3832680
hg1932680
hg1832680
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891930
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782522
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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