A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16918362



Internal ID13007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:120752437..120800697hg38UCSC Ensembl
chr2:121510013..121558273hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg3848261
hg1948261
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5451233
Supporting Variants
Samples
Known GenesGLI2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16918362
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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