A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800346



Internal ID19167353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52438287..52733078hg38UCSC Ensembl
Innerchr19:52941540..53236331hg19UCSC Ensembl
Innerchr19:57633352..57928143hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38294792
hg19294792
hg18294792
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893233
Supporting Variants
Samples
Known GenesZNF137P, ZNF534, ZNF578, ZNF611, ZNF701, ZNF808, ZNF83
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=63
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800346
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