A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891361



Internal ID19185757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16611256..16719048hg38UCSC Ensembl
Outerchr8:16530356..16735092hg38UCSC Ensembl
Innerchr8:16468765..16576557hg19UCSC Ensembl
Outerchr8:16387865..16592601hg19UCSC Ensembl
Innerchr8:16513136..16620928hg18UCSC Ensembl
Outerchr8:16432236..16636972hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38204737
hg19204737
hg18204737
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782652, essv25790163
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891361
Frequency
Sample Size3017
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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