A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16922476



Internal ID15747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:182552426..182554196hg38UCSC Ensembl
chr2:183417153..183418923hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg381771
hg191771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435611
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16922476
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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