A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5963615



Internal ID8941019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46754014..46809682hg38UCSC Ensembl
chr3:46795504..46851172hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3855669
hg1955669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660220
Supporting Variants
SamplesNA19319
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5963615
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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