A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17690423



Internal ID114089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102562195..102602104hg38UCSC Ensembl
chr12:102955973..102995882hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg3839910
hg1939910
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5494611
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17690423
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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