A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16912667



Internal ID9190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:47760869..47761928hg38UCSC Ensembl
chr2:47988008..47989067hg19UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg381060
hg191060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5434225
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16912667
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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