A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv858e199



Internal ID22758631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41114495..41119964hg38UCSC Ensembl
chr3:41155986..41161455hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg385470
hg195470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2661277, esv2674239
SamplesNA19390
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv858e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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