A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025884



Internal ID84993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65521900..65538100hg38UCSC Ensembl
chr9:44798635..44814756hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3816201
hg1916122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486173
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025884
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.157071


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