A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660187



Internal ID9926292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81466218..81470253hg38UCSC Ensembl
chr8:82378453..82382488hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg384036
hg194036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6543365
SamplesNA19700
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660187
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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