A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415438



Internal ID194695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90708224..90708275hg38UCSC Ensembl
chr13:91360478..91360529hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17694362
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415438
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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