A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675250



Internal ID9941355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:98422034..98432749hg38UCSC Ensembl
Outerchr3:98422000..98432784hg38UCSC Ensembl
Innerchr3:98140878..98151593hg19UCSC Ensembl
Outerchr3:98140844..98151628hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3810785
hg1910785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv874e199
Supporting Variantsessv5595348
SamplesNA18565
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675250
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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