A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619848



Internal ID7006722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17582182..17636018hg38UCSC Ensembl
chr9:17582180..17636016hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3853837
hg1953837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1457e214
Supporting Variantsessv13412192, essv13412191
SamplesNA12287, HG00157
Known GenesSH3GL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619848
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer