A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3410409



Internal ID15257369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65206458..65217747hg38UCSC Ensembl
Innerchr9:65207447..65216747hg38UCSC Ensembl
Outerchr9:65205432..65218747hg38UCSC Ensembl
chr9:42784856..42795854hg19UCSC Ensembl
Innerchr9:42785856..42794854hg19UCSC Ensembl
Outerchr9:42783856..42796854hg19UCSC Ensembl
chr9:42774852..42785850hg18UCSC Ensembl
Innerchr9:42775852..42784850hg18UCSC Ensembl
Outerchr9:42773852..42786850hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3811290
hg1910999
hg1810999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4339e59
Supporting Variantsessv8696754
SamplesNA12892
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3410409
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