A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5539190



Internal ID314166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:101234764..101234801hg38UCSC Ensembl
chr12:101628542..101628579hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17690348
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5539190
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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