A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669678



Internal ID9935783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:95150494..95150968hg38UCSC Ensembl
Outerchr11:95150337..95151121hg38UCSC Ensembl
Innerchr11:94883658..94884132hg19UCSC Ensembl
Outerchr11:94883501..94884285hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38785
hg19785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6242596, essv5532269, essv6328980, essv6453111
SamplesNA19700, NA20766, NA19347, NA19380
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669678
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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