A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783012



Internal ID18819029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6500395..6763100hg38UCSC Ensembl
Innerchr3:6542082..6804787hg19UCSC Ensembl
Innerchr3:6517082..6779787hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38262706
hg19262706
hg18262706
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893652
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=68
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783012
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