A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455862



Internal ID233934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87696470..87696747hg38UCSC Ensembl
chr6:88406188..88406465hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985015
Samples
Known GenesAKIRIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455862
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