A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5409162



Internal ID188484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149228555..149228606hg38UCSC Ensembl
chr6:149549691..149549742hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16988973
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5409162
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