A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3397224



Internal ID15244187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135990705..135990958hg38UCSC Ensembl
Innerchr9:135990705..135990958hg38UCSC Ensembl
Outerchr9:135990438..135991473hg38UCSC Ensembl
chr9:138882551..138882804hg19UCSC Ensembl
Innerchr9:138882551..138882804hg19UCSC Ensembl
Outerchr9:138882284..138883319hg19UCSC Ensembl
chr9:138022372..138022625hg18UCSC Ensembl
Innerchr9:138022372..138022625hg18UCSC Ensembl
Outerchr9:138022105..138023140hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38254
hg19254
hg18254
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8652427
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3397224
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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