A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934177



Internal ID22709498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79606241..79606614hg38UCSC Ensembl
chr16:79640138..79640511hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383923
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934177
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