A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17057795



Internal ID106386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56863718..56885777hg38UCSC Ensembl
chr12:57257502..57279561hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg3822060
hg1922060
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5499112
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17057795
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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