A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666090



Internal ID9932195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149029820..149030672hg38UCSC Ensembl
chr6:149350956..149351808hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38853
hg19853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5948911, essv6151445, essv6326918, essv5881061
SamplesNA18856, NA18853, NA19099, NA19835
Known GenesUST
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666090
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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