A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17058252



Internal ID106698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:49202643..49207158hg38UCSC Ensembl
chr12:49596426..49600941hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg384516
hg194516
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510784
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17058252
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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