A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5417084



Internal ID196289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100637968..100638019hg38UCSC Ensembl
chr15:101178173..101178224hg19UCSC Ensembl
Cytoband15q26.3
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 Variantsnssv17703861
Samples
Known GenesASB7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5417084
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