A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796025



Internal ID19180650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:11438322..11459215hg38UCSC Ensembl
Innerchr4:11439946..11460839hg19UCSC Ensembl
Innerchr4:11049044..11069937hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3820894
hg1920894
hg1820894
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893881
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796025
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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