A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17840435



Internal ID22024078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:141145828..141145828hg38UCSC Ensembl
chr8:142155927..142155927hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6246750
Supporting Variants
Samples
Known GenesDENND3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17840435
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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