A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779739



Internal ID19180899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:28187430..28238686hg38UCSC Ensembl
Innerchr19:28678337..28729593hg19UCSC Ensembl
Innerchr19:33370177..33421433hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3851257
hg1951257
hg1851257
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893197
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779739
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