A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17690902



Internal ID114568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124723656..124724841hg38UCSC Ensembl
chr12:125208202..125209387hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg381186
hg191186
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503448
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17690902
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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