A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801275



Internal ID19170802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:7940396..8028581hg38UCSC Ensembl
Innerchr3:7982083..8070268hg19UCSC Ensembl
Innerchr3:7957083..8045268hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3888186
hg1988186
hg1888186
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893660
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=26
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801275
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