A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937111



Internal ID25455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100618214..100624584hg38UCSC Ensembl
chr3:100337058..100343428hg19UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg386371
hg196371
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449796
Supporting Variants
Samples
Known GenesGPR128
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937111
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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