A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16923923



Internal ID16710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:222266496..222266528hg38UCSC Ensembl
chr2:223131215..223131247hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5550268
Supporting Variants
Samples
Known GenesPAX3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16923923
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00281


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