A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677416



Internal ID9943521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:113044959..113047242hg38UCSC Ensembl
Outerchr3:113044922..113047292hg38UCSC Ensembl
Innerchr3:112763806..112766089hg19UCSC Ensembl
Outerchr3:112763769..112766139hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg382371
hg192371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv880e199
Supporting Variantsessv5707886
SamplesHG01149
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677416
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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