A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027190



Internal ID85844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123686678..123690196hg38UCSC Ensembl
chr9:126448957..126452475hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg383519
hg193519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480698
Supporting Variants
Samples
Known GenesDENND1A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027190
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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