A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677849



Internal ID9943954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:36576900..36581069hg38UCSC Ensembl
Outerchr8:36576863..36581119hg38UCSC Ensembl
Innerchr8:36434418..36438587hg19UCSC Ensembl
Outerchr8:36434381..36438637hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg384257
hg194257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1281e199
Supporting Variantsessv5402527
SamplesNA18546
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677849
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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