A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv889e214



Internal ID22756783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43663965..43677052hg38UCSC Ensembl
chr3:43705457..43718544hg19UCSC Ensembl
Cytoband3p21.33
Allele length
AssemblyAllele length
hg3813088
hg1913088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3596020, esv3596022
SamplesNA19025
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv889e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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