A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5421559



Internal ID200627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30615367..30615418hg38UCSC Ensembl
chr13:31189504..31189555hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686602
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5421559
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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