A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697116



Internal ID15060861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63304160..63313758hg38UCSC Ensembl
Innerchr9:63305160..63312758hg38UCSC Ensembl
Outerchr9:63303160..63314758hg38UCSC Ensembl
chr9:67259132..67268730hg19UCSC Ensembl
Innerchr9:67260132..67267730hg19UCSC Ensembl
Outerchr9:67258132..67269730hg19UCSC Ensembl
chr9:66948952..66958550hg18UCSC Ensembl
Innerchr9:66949952..66957550hg18UCSC Ensembl
Outerchr9:66947952..66959550hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg389599
hg199599
hg189599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3384405
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697116
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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