A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664959



Internal ID9931064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:47482794..47491678hg38UCSC Ensembl
Outerchr3:47482757..47491728hg38UCSC Ensembl
Innerchr3:47524284..47533168hg19UCSC Ensembl
Outerchr3:47524247..47533218hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg388972
hg198972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv861e199
Supporting Variantsessv5444894, essv5662663, essv5889805
SamplesNA19448, NA19445, NA19346
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664959
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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