A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892074



Internal ID19186470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:95014972..95048683hg38UCSC Ensembl
Outerchr11:95014972..95059226hg38UCSC Ensembl
Innerchr11:94748136..94781847hg19UCSC Ensembl
Outerchr11:94748136..94792390hg19UCSC Ensembl
Innerchr11:94387784..94421495hg18UCSC Ensembl
Outerchr11:94387784..94432038hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3844255
hg1944255
hg1844255
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778740, essv25796950, essv25785411
Samples
Known GenesKDM4E
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892074
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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