A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800874



Internal ID18831308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:57645..289329hg38UCSC Ensembl
Innerchr4:57538..283118hg19UCSC Ensembl
Innerchr4:47538..273118hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38231685
hg19225581
hg18225581
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893860
Supporting Variants
Samples
Known GenesZNF595, ZNF718, ZNF732, ZNF876P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=36
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800874
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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