A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796817



Internal ID19172916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34108692..34229433hg38UCSC Ensembl
Innerchr4:34110314..34231055hg19UCSC Ensembl
Innerchr4:33786709..33907450hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38120742
hg19120742
hg18120742
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893910
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796817
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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