A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796263



Internal ID19181908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:25212651..25440874hg38UCSC Ensembl
Innerchr9:25212649..25440872hg19UCSC Ensembl
Innerchr9:25202649..25430872hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38228224
hg19228224
hg18228224
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891642
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=50
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796263
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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