A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5414990



Internal ID194255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40840626..40840677hg38UCSC Ensembl
chr15:41132824..41132875hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700144
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5414990
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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