A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17055583



Internal ID104889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32420529..32453821hg38UCSC Ensembl
chr12:32573463..32606755hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3833293
hg1933293
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5509280
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17055583
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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