A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv914e214



Internal ID22756808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98421929..98432680hg38UCSC Ensembl
chr3:98140773..98151524hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3810752
hg1910752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3597116, esv3597115
SamplesNA18565
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv914e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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