A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791077



Internal ID19177058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:14762811..15157646hg38UCSC Ensembl
Innerchr8:14620320..15015155hg19UCSC Ensembl
Innerchr8:14664691..15059526hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38394836
hg19394836
hg18394836
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891347
Supporting Variants
Samples
Known GenesMIR383, SGCZ
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=325
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791077
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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