A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5412178



Internal ID191482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49685840..49685891hg38UCSC Ensembl
chr6:49653553..49653604hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16983260
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5412178
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