A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893861



Internal ID18837995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:17764..156885hg38UCSC Ensembl
Outerchr4:17764..156885hg38UCSC Ensembl
Innerchr4:17764..150683hg19UCSC Ensembl
Outerchr4:17764..150683hg19UCSC Ensembl
Innerchr4:7764..140683hg18UCSC Ensembl
Outerchr4:7764..140683hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38139122
hg19132920
hg18132920
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792795
Samples
Known GenesZNF595, ZNF718
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893861
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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