A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885163



Internal ID22660148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32319948..32320630hg38UCSC Ensembl
chr1:32785549..32786231hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38683
hg19683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372214
Samples
Known GenesHDAC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885163
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