A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697115



Internal ID15103413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63304160..63311358hg38UCSC Ensembl
Innerchr9:63305160..63310358hg38UCSC Ensembl
Outerchr9:63303160..63312358hg38UCSC Ensembl
chr9:67259132..67266330hg19UCSC Ensembl
Innerchr9:67260132..67265330hg19UCSC Ensembl
Outerchr9:67258132..67267330hg19UCSC Ensembl
chr9:66948952..66956150hg18UCSC Ensembl
Innerchr9:66949952..66955150hg18UCSC Ensembl
Outerchr9:66947952..66957150hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg387199
hg197199
hg187199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3330487
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697115
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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