A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16939634



Internal ID27143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136217681..136217714hg38UCSC Ensembl
chr3:135936523..135936556hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5543324
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16939634
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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