A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893860



Internal ID18837994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:75090..225749hg38UCSC Ensembl
Outerchr4:57645..289329hg38UCSC Ensembl
Innerchr4:74983..219538hg19UCSC Ensembl
Outerchr4:57538..283118hg19UCSC Ensembl
Innerchr4:64983..209538hg18UCSC Ensembl
Outerchr4:47538..273118hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38231685
hg19225581
hg18225581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800874, essv25781968
Samples
Known GenesZNF595, ZNF718, ZNF732, ZNF876P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893860
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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