A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3415932



Internal ID15262891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95556849..95558247hg38UCSC Ensembl
Innerchr9:95557247..95557849hg38UCSC Ensembl
Outerchr9:95555849..95559247hg38UCSC Ensembl
chr9:98319131..98320529hg19UCSC Ensembl
Innerchr9:98319529..98320131hg19UCSC Ensembl
Outerchr9:98318131..98321529hg19UCSC Ensembl
chr9:97358952..97360350hg18UCSC Ensembl
Innerchr9:97359952..97359350hg18UCSC Ensembl
Outerchr9:97357952..97361350hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8697438
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3415932
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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