A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3894020



Internal ID19184874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121587499..121651899hg38UCSC Ensembl
Outerchr4:121561423..121656615hg38UCSC Ensembl
Innerchr4:122508654..122573054hg19UCSC Ensembl
Outerchr4:122482578..122577770hg19UCSC Ensembl
Innerchr4:122728104..122792504hg18UCSC Ensembl
Outerchr4:122702028..122797220hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3895193
hg1995193
hg1895193
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791299, essv25792203
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3894020
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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