A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424960



Internal ID203934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39519562..39519562hg38UCSC Ensembl
chr15:39811763..39811763hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700083
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424960
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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