A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791893



Internal ID18814246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:48711661..49369067hg38UCSC Ensembl
Innerchr11:48733213..49390619hg19UCSC Ensembl
Innerchr11:48689789..49347195hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38657407
hg19657407
hg18657407
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891984
Supporting Variants
Samples
Known GenesFOLH1, TRIM49B, TRIM64C
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=100
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791893
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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