A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17057384



Internal ID106101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25431199..25431199hg38UCSC Ensembl
chr12:25584133..25584133hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5541438
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17057384
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.095395


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