A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666950



Internal ID9586369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:98044032..98052329hg38UCSC Ensembl
Outerchr9:98043995..98052379hg38UCSC Ensembl
Innerchr9:100806314..100814611hg19UCSC Ensembl
Outerchr9:100806277..100814661hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg388385
hg198385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6254074
SamplesNA19138
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666950
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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