A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796308



Internal ID18835934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42130892..42138944hg38UCSC Ensembl
Innerchr15:42423090..42431142hg19UCSC Ensembl
Innerchr15:40210382..40218434hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg388053
hg198053
hg188053
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892678
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796308
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer