A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902086



Internal ID22677240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28089446..28089511hg38UCSC Ensembl
chr6:28057224..28057289hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429648
Samples
Known GenesZNF165
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902086
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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