A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936970



Internal ID25360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94025229..94025275hg38UCSC Ensembl
chr3:93744073..93744119hg19UCSC Ensembl
Cytoband3q11.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5550681
Supporting Variants
Samples
Known GenesARL13B, STX19
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936970
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001873


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