A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796041



Internal ID19164279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:120285335..120484900hg38UCSC Ensembl
Innerchr4:121206490..121406055hg19UCSC Ensembl
Innerchr4:121425940..121625505hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg38199566
hg19199566
hg18199566
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894017
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=27
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796041
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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