A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621634



Internal ID7008502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:119397495..119466740hg38UCSC Ensembl
chr9:122159773..122229018hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3869246
hg1969246
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13613192
SamplesHG02419
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621634
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