A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936396



Internal ID24989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112354222..112354329hg38UCSC Ensembl
chr3:112073069..112073176hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5439989
Supporting Variants
Samples
Known GenesCD200
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936396
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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