A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619913



Internal ID6660099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19433835..19551230hg38UCSC Ensembl
chr9:19433833..19551228hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg38117396
hg19117396
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13415355, essv13415356
SamplesHG03490, NA19328
Known GenesACER2, SLC24A2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619913
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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