A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12065340



Internal ID5356603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133790833..133795185hg38UCSC Ensembl
chr5:133126524..133130876hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg384353
hg194353
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3606829
Supporting Variants
SamplesNA18907
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12065340
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer