A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932298



Internal ID22707594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48967871..48968262hg38UCSC Ensembl
chr16:49001782..49002173hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373593
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932298
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