A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893963



Internal ID19184817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:72701253..72863345hg38UCSC Ensembl
Outerchr4:72701253..72863345hg38UCSC Ensembl
Innerchr4:73566970..73729062hg19UCSC Ensembl
Outerchr4:73566970..73729062hg19UCSC Ensembl
Innerchr4:73785834..73947926hg18UCSC Ensembl
Outerchr4:73785834..73947926hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38162093
hg19162093
hg18162093
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790664
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893963
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