A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1426e214



Internal ID22757320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:141120386..141147214hg38UCSC Ensembl
chr8:142130485..142157313hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3826829
hg1926829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3619052, esv3619051
SamplesHG02836, HG00182
Known GenesDENND3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1426e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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