A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668823



Internal ID9934928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29080613..29109604hg38UCSC Ensembl
Outerchr9:29080576..29109654hg38UCSC Ensembl
Innerchr9:29080611..29109602hg19UCSC Ensembl
Outerchr9:29080574..29109652hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3829079
hg1929079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5499387
SamplesHG00472
Known GenesLINGO2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668823
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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