A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16930811



Internal ID21291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9490035..9490110hg38UCSC Ensembl
chr3:9531719..9531794hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443596
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16930811
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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