A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551806



Internal ID325230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40386249..40386286hg38UCSC Ensembl
chr15:40678450..40678487hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700114
Samples
Known GenesKNSTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551806
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