A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661277



Internal ID9927382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41114520..41119942hg38UCSC Ensembl
chr3:41156011..41161433hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg385423
hg195423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv858e199
Supporting Variantsessv5421800
SamplesNA19390
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661277
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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