A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792795



Internal ID18835122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:17764..156885hg38UCSC Ensembl
Innerchr4:17764..150683hg19UCSC Ensembl
Innerchr4:7764..140683hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38139122
hg19132920
hg18132920
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893861
Supporting Variants
Samples
Known GenesZNF595, ZNF718
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792795
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer