A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661173



Internal ID9927278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:123755488..123762395hg38UCSC Ensembl
Outerchr8:123755331..123762548hg38UCSC Ensembl
Innerchr8:124767728..124774635hg19UCSC Ensembl
Outerchr8:124767571..124774788hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg387218
hg197218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6484792
SamplesNA18622
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661173
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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