A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16918633



Internal ID13188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105221683..105224257hg38UCSC Ensembl
chr2:105838140..105840714hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg382575
hg192575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443751
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16918633
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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