A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5416731



Internal ID195948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91130148..91130199hg38UCSC Ensembl
chr15:91673378..91673429hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705140
Samples
Known GenesSV2B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5416731
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer