A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660843



Internal ID9926948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:178364031..178418742hg38UCSC Ensembl
chr3:178081819..178136530hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3854712
hg1954712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5603380, essv5496635
SamplesNA19374, NA19373
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660843
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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