A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16922497



Internal ID15761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:171910917..171916303hg38UCSC Ensembl
chr2:172767427..172772813hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg385387
hg195387
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5441719
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16922497
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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