A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800581



Internal ID18827328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34380017..34515668hg38UCSC Ensembl
Innerchr15:34672218..34807869hg19UCSC Ensembl
Innerchr15:32459510..32595161hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38135652
hg19135652
hg18135652
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892664
Supporting Variants
Samples
Known GenesGOLGA8A, MIR1233-1, MIR1233-2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800581
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