A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659041



Internal ID9925146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98422026..98432775hg38UCSC Ensembl
chr3:98140870..98151619hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3810750
hg1910750
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv874e199
Supporting Variantsessv6408184
SamplesNA18565
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659041
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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