A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619052



Internal ID7005933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:141120796..141147214hg38UCSC Ensembl
chr8:142130895..142157313hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3826419
hg1926419
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1426e214
Supporting Variantsessv13358379
SamplesHG02836
Known GenesDENND3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619052
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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