A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789881



Internal ID18822517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49916027..50771311hg38UCSC Ensembl
Innerchr11:49937579..50730482hg19UCSC Ensembl
Innerchr11:49894155..50687058hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38855285
hg19792904
hg18792904
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892002
Supporting Variants
Samples
Known GenesLOC441601, LOC646813, OR4C12, OR4C13
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=98
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789881
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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