A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415407



Internal ID194663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107094578..107094624hg38UCSC Ensembl
chr13:107746926..107746972hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17692366
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415407
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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