A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891620



Internal ID19186016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:16051492..16074728hg38UCSC Ensembl
Outerchr9:16051492..16074728hg38UCSC Ensembl
Innerchr9:16051490..16074726hg19UCSC Ensembl
Outerchr9:16051490..16074726hg19UCSC Ensembl
Innerchr9:16041490..16064726hg18UCSC Ensembl
Outerchr9:16041490..16064726hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3823237
hg1923237
hg1823237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796964
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891620
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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