A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16937714



Internal ID25851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:131005750..131005801hg38UCSC Ensembl
chr3:130724594..130724645hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5413135
Supporting Variants
Samples
Known GenesATP2C1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16937714
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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