A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891398



Internal ID19185794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:55878090..56029138hg38UCSC Ensembl
Outerchr8:55878090..56029138hg38UCSC Ensembl
Innerchr8:56790649..56941697hg19UCSC Ensembl
Outerchr8:56790649..56941697hg19UCSC Ensembl
Innerchr8:56953203..57104251hg18UCSC Ensembl
Outerchr8:56953203..57104251hg18UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38151049
hg19151049
hg18151049
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792813
Samples
Known GenesLYN
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891398
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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