A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786290



Internal ID19165720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:72178436..72192971hg38UCSC Ensembl
Innerchr3:72227587..72242122hg19UCSC Ensembl
Innerchr3:72310277..72324812hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3814536
hg1914536
hg1814536
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893721
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786290
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