A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792813



Internal ID19159671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:55878090..56029138hg38UCSC Ensembl
Innerchr8:56790649..56941697hg19UCSC Ensembl
Innerchr8:56953203..57104251hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38151049
hg19151049
hg18151049
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891398
Supporting Variants
Samples
Known GenesLYN
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=45
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792813
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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