A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5535955



Internal ID311525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60357512..60357547hg38UCSC Ensembl
chr13:60931646..60931681hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17688270
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5535955
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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