A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427722



Internal ID22485592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:33391877..33394887hg38UCSC Ensembl
chr5:33391983..33394993hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg383011
hg193011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5905168
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427722
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