A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11191899



Internal ID686155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155760377..155780857hg38UCSC Ensembl
chr3:155478166..155498646hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3820481
hg1920481
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3598285
Supporting Variants
SamplesHG00323
Known GenesC3orf33
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11191899
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