A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891984



Internal ID18839694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:48829035..49315286hg38UCSC Ensembl
Outerchr11:48711661..49369067hg38UCSC Ensembl
Innerchr11:48850587..49336838hg19UCSC Ensembl
Outerchr11:48733213..49390619hg19UCSC Ensembl
Innerchr11:48807163..49293414hg18UCSC Ensembl
Outerchr11:48689789..49347195hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38657407
hg19657407
hg18657407
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791893, essv25790937
Samples
Known GenesFOLH1, TRIM49B, TRIM64C
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891984
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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