A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13481168



Internal ID3264551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61197633..61208600hg38UCSC Ensembl
chr9:43612172..43623150hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3810968
hg1910979
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620476
Supporting Variants
SamplesHG02884
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13481168
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