A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422940



Internal ID201968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91308564..91308615hg38UCSC Ensembl
chr15:91851794..91851845hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17703626
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422940
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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