A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16039955



Internal ID4628763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31887650..31896396hg38UCSC Ensembl
chr19:32378556..32387302hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg388747
hg198747
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644155
Supporting Variants
SamplesHG04159
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16039955
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