A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3362844



Internal ID15209822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68220553..68236714hg38UCSC Ensembl
Innerchr9:68221516..68235714hg38UCSC Ensembl
Outerchr9:68220553..68237714hg38UCSC Ensembl
chr9:70835469..70851630hg19UCSC Ensembl
Innerchr9:70836432..70850630hg19UCSC Ensembl
Outerchr9:70835469..70852630hg19UCSC Ensembl
chr9:70025252..70041450hg18UCSC Ensembl
Innerchr9:70026252..70040450hg18UCSC Ensembl
Outerchr9:70024252..70042450hg18UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3816162
hg1916162
hg1816199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697368
SamplesNA12878
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3362844
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