A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3328394



Internal ID15175380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98873699..98873712hg38UCSC Ensembl
Innerchr9:98873704..98873707hg38UCSC Ensembl
Outerchr9:98873694..98873717hg38UCSC Ensembl
chr9:101635981..101635994hg19UCSC Ensembl
Innerchr9:101635986..101635989hg19UCSC Ensembl
Outerchr9:101635976..101635999hg19UCSC Ensembl
chr9:100675802..100675815hg18UCSC Ensembl
Innerchr9:100675807..100675810hg18UCSC Ensembl
Outerchr9:100675797..100675820hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7864955
SamplesNA12005
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3328394
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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