A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797907



Internal ID18819407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20792030..20932790hg38UCSC Ensembl
Innerchr15:20997359..21138119hg19UCSC Ensembl
Innerchr15:19257404..19402778hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38140761
hg19140761
hg18145375
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892629
Supporting Variants
Samples
Known GenesCXADRP2, NF1P2, POTEB, POTEB2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797907
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