A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778740



Internal ID19160691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:95014972..95048683hg38UCSC Ensembl
Innerchr11:94748136..94781847hg19UCSC Ensembl
Innerchr11:94387784..94421495hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3833712
hg1933712
hg1833712
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892074
Supporting Variants
Samples
Known GenesKDM4E
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778740
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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