A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5497402



Internal ID274437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:21396650..21418650hg38UCSC Ensembl
chr12:21549584..21571584hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3822001
hg1922001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17053975
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5497402
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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