A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796721



Internal ID19163769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:19074255..19200196hg38UCSC Ensembl
Innerchr4:19075878..19201819hg19UCSC Ensembl
Innerchr4:18684976..18810917hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38125942
hg19125942
hg18125942
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893892
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796721
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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