A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663747



Internal ID9929852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84024920..84029554hg38UCSC Ensembl
chr6:84734639..84739273hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg384635
hg194635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6475503, essv5428836
SamplesHG01072, NA19129
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663747
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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