A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17057452



Internal ID106142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:28776221..28778887hg38UCSC Ensembl
chr12:28929154..28931820hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg382667
hg192667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500525
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17057452
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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