A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3394460



Internal ID15241425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92803749..92805347hg38UCSC Ensembl
Innerchr9:92804347..92804749hg38UCSC Ensembl
Outerchr9:92802749..92806347hg38UCSC Ensembl
chr9:95566031..95567629hg19UCSC Ensembl
Innerchr9:95566629..95567031hg19UCSC Ensembl
Outerchr9:95565031..95568629hg19UCSC Ensembl
chr9:94605852..94607450hg18UCSC Ensembl
Innerchr9:94606852..94606450hg18UCSC Ensembl
Outerchr9:94604852..94608450hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg381599
hg191599
hg181599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4481e59
Supporting Variantsessv8697429
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3394460
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