A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670446



Internal ID9936551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:162292614..162308441hg38UCSC Ensembl
chr3:162010402..162026229hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3815828
hg1915828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6054910
SamplesNA06984
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670446
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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