A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791519



Internal ID19177327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15562268..15574673hg38UCSC Ensembl
Innerchr8:15419777..15432182hg19UCSC Ensembl
Innerchr8:15464148..15476553hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3812406
hg1912406
hg1812406
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891352
Supporting Variants
Samples
Known GenesTUSC3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=11
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791519
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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