A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027210



Internal ID85860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123913683..123919667hg38UCSC Ensembl
chr9:126675962..126681946hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385985
hg195985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475896
Supporting Variants
Samples
Known GenesDENND1A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027210
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002811


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