A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891642



Internal ID19186038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25212651..25440874hg38UCSC Ensembl
Outerchr9:25212651..25440874hg38UCSC Ensembl
Innerchr9:25212649..25440872hg19UCSC Ensembl
Outerchr9:25212649..25440872hg19UCSC Ensembl
Innerchr9:25202649..25430872hg18UCSC Ensembl
Outerchr9:25202649..25430872hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38228224
hg19228224
hg18228224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25796263
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891642
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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