A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5962884



Internal ID22737819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:31593167..31594312hg38UCSC Ensembl
chr20:30180970..30182115hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg381146
hg191146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389867
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5962884
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