A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785411



Internal ID19166272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:95014972..95059226hg38UCSC Ensembl
Innerchr11:94748136..94792390hg19UCSC Ensembl
Innerchr11:94387784..94432038hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3844255
hg1944255
hg1844255
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=15
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785411
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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