A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16938845



Internal ID26619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140096871..140096871hg38UCSC Ensembl
chr3:139815713..139815713hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538773
Supporting Variants
Samples
Known GenesCLSTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16938845
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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