A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663032



Internal ID9582451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:32384957..32390557hg38UCSC Ensembl
Outerchr8:32384920..32390607hg38UCSC Ensembl
Innerchr8:32242473..32248073hg19UCSC Ensembl
Outerchr8:32242436..32248123hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg385688
hg195688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5420250
SamplesNA18959
Known GenesNRG1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663032
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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