A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456613



Internal ID234675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106559419..106560777hg38UCSC Ensembl
chr6:107007294..107008652hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381359
hg191359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735600
Samples
Known GenesAIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456613
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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