A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668117



Internal ID9587536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16087879..16166357hg38UCSC Ensembl
Outerchr8:16087842..16166407hg38UCSC Ensembl
Innerchr8:15945388..16023866hg19UCSC Ensembl
Outerchr8:15945351..16023916hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3878566
hg1978566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5901238
SamplesHG00337
Known GenesMSR1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668117
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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