A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5549132



Internal ID322825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104385575..104385588hg38UCSC Ensembl
chr12:104779353..104779366hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17690527
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5549132
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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