A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3424422



Internal ID15271379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39809734..39814432hg38UCSC Ensembl
Innerchr9:39810734..39813432hg38UCSC Ensembl
Outerchr9:39808734..39815432hg38UCSC Ensembl
chr9:41954752..41959450hg19UCSC Ensembl
Innerchr9:41955752..41958450hg19UCSC Ensembl
Outerchr9:41953752..41960450hg19UCSC Ensembl
chr9:41944752..41949450hg18UCSC Ensembl
Innerchr9:41945752..41948450hg18UCSC Ensembl
Outerchr9:41943752..41950450hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg384699
hg194699
hg184699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8696652
SamplesNA19240
Known GenesKGFLP2, MGC21881
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3424422
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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