A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662130



Internal ID9928235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:70009239..70018184hg38UCSC Ensembl
chr3:70058390..70067335hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg388946
hg198946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5951385, essv5653500
SamplesHG01070, HG00464
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662130
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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