A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665708



Internal ID9931813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:20702665..20725368hg38UCSC Ensembl
Outerchr8:20702628..20725418hg38UCSC Ensembl
Innerchr8:20560176..20582879hg19UCSC Ensembl
Outerchr8:20560139..20582929hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3822791
hg1922791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6509908
SamplesHG00692
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665708
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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