A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3385755



Internal ID15232725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63304160..63314158hg38UCSC Ensembl
Innerchr9:63305160..63313158hg38UCSC Ensembl
Outerchr9:63303160..63315158hg38UCSC Ensembl
chr9:67259132..67269130hg19UCSC Ensembl
Innerchr9:67260132..67268130hg19UCSC Ensembl
Outerchr9:67258132..67270130hg19UCSC Ensembl
chr9:66948952..66958950hg18UCSC Ensembl
Innerchr9:66949952..66957950hg18UCSC Ensembl
Outerchr9:66947952..66959950hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg389999
hg199999
hg189999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4398e59
Supporting Variantsessv8697117
SamplesNA12878
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3385755
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