A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791187



Internal ID18820897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:19744844..20118728hg38UCSC Ensembl
Innerchr8:19602355..19976239hg19UCSC Ensembl
Innerchr8:19646635..20020519hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38373885
hg19373885
hg18373885
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891372
Supporting Variants
Samples
Known GenesINTS10, LPL
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=104
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791187
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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