A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910852



Internal ID8003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19628015..19636584hg38UCSC Ensembl
chr2:19827776..19836345hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg388570
hg198570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5449389
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910852
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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