A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16927224



Internal ID18860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:242166047..242174047hg38UCSC Ensembl
chr16:90287654..90294753hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg388001
hg197100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140036
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16927224
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.196429


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