A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16923634



Internal ID16524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:197356650..197357514hg38UCSC Ensembl
chr2:198221374..198222238hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38865
hg19865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438995
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16923634
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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