A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16928047



Internal ID19402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:208215556..208216408hg38UCSC Ensembl
chr2:209080280..209081132hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38853
hg19853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5437190
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16928047
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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