A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661068



Internal ID9927173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:9393841..9396442hg38UCSC Ensembl
Outerchr1:9393804..9396492hg38UCSC Ensembl
Innerchr1:9453900..9456501hg19UCSC Ensembl
Outerchr1:9453863..9456551hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg382689
hg192689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6347520
SamplesNA18530
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661068
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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