A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892600



Internal ID19183420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20367552..20418387hg38UCSC Ensembl
Outerchr15:20357034..20418387hg38UCSC Ensembl
Innerchr15:20572805..20623640hg19UCSC Ensembl
Outerchr15:20562287..20623640hg19UCSC Ensembl
Innerchr15:18832819..18883654hg18UCSC Ensembl
Outerchr15:18822301..18883654hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3861354
hg1961354
hg1861354
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782713, essv25786942, essv25786140, essv25799510, essv25786334, essv25785929, essv25785729
Samples
Known GenesHERC2P3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892600
Frequency
Sample Size3017
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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