A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16928219



Internal ID19512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218410455..218424867hg38UCSC Ensembl
chr2:219275178..219289590hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3814413
hg1914413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453454
Supporting Variants
Samples
Known GenesVIL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16928219
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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