A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8696746



Internal ID13658698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65259174..65280788hg38UCSC Ensembl
Innerchr9:65260178..65279788hg38UCSC Ensembl
Outerchr9:65258287..65281787hg38UCSC Ensembl
chr9:42721656..42743254hg19UCSC Ensembl
Innerchr9:42722656..42742254hg19UCSC Ensembl
Outerchr9:42720656..42744254hg19UCSC Ensembl
chr9:42711652..42733250hg18UCSC Ensembl
Innerchr9:42712652..42732250hg18UCSC Ensembl
Outerchr9:42710652..42734250hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3821615
hg1921599
hg1821599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3394418
Supporting Variants
SamplesNA12878
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8696746
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