A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17689441



Internal ID113107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:80030537..80030618hg38UCSC Ensembl
chr12:80424317..80424398hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6143710
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17689441
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.016378


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