A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782823



Internal ID18819838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34402116..34496365hg38UCSC Ensembl
Innerchr15:34694317..34788566hg19UCSC Ensembl
Innerchr15:32481609..32575858hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3894250
hg1994250
hg1894250
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892664
Supporting Variants
Samples
Known GenesGOLGA8A
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782823
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