A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5508689



Internal ID285376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43512279..43512345hg38UCSC Ensembl
chr15:43804477..43804543hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702015
Samples
Known GenesRNU6-28P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5508689
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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