A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666658



Internal ID9932763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89136169..89141974hg38UCSC Ensembl
chr6:89845888..89851693hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg385806
hg195806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5449224
SamplesHG00500
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666658
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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