A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535327



Internal ID310977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:87429146..87429155hg38UCSC Ensembl
chr12:87822923..87822932hg19UCSC Ensembl
Cytoband12q21.32
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17689871
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535327
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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