A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667885



Internal ID9933990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:152081355..152082112hg38UCSC Ensembl
Outerchr3:152081318..152082162hg38UCSC Ensembl
Innerchr3:151799144..151799901hg19UCSC Ensembl
Outerchr3:151799107..151799951hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38845
hg19845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5682839
SamplesNA18574
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667885
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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