A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025984



Internal ID85056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77711977..77717266hg38UCSC Ensembl
chr9:80326893..80332182hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg385290
hg195290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479589
Supporting Variants
Samples
Known GenesGNAQ
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025984
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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