A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023661



Internal ID83486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35578824..35578927hg38UCSC Ensembl
chr9:35578821..35578924hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482616
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023661
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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