A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792830



Internal ID18819017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:49969942..50273586hg38UCSC Ensembl
Innerchr11:49991492..50232757hg19UCSC Ensembl
Innerchr11:49948068..50189333hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38303645
hg19241266
hg18241266
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892003
Supporting Variants
Samples
Known GenesOR4C12
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=37
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792830
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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