A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666824



Internal ID9932929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14379765..14380910hg38UCSC Ensembl
chr6:14379996..14381141hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381146
hg191146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5875968, essv6261467, essv6290697, essv6190984
SamplesNA18977, HG00479, NA18576, NA18546
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666824
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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