A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023461



Internal ID83358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32659146..32665175hg38UCSC Ensembl
chr9:32659144..32665173hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg386030
hg196030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476403
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023461
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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