A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16929510



Internal ID20402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13348910..13349050hg38UCSC Ensembl
chr3:13390410..13390550hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5445095
Supporting Variants
Samples
Known GenesNUP210
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16929510
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.17112


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