A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898532



Internal ID22673648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13489813..13490993hg38UCSC Ensembl
chr3:13531313..13532493hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg381181
hg191181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404926
Samples
Known GenesHDAC11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898532
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