A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16920829



Internal ID14662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:145761751..145761802hg38UCSC Ensembl
chr2:146519319..146519370hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5546978
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16920829
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00359


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