A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563918



Internal ID336843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60913127..60913178hg38UCSC Ensembl
chr15:61205326..61205377hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg382819
hg192819
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703188
Samples
Known GenesRORA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563918
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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