A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv874e199



Internal ID22758647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98422000..98432784hg38UCSC Ensembl
chr3:98140844..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 Variants
Supporting Variantsesv2675250, esv2659041
SamplesNA18565
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv874e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer