A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17383923



Internal ID22441793
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 StatusS
Merged Variantsnsv5934177
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17383923
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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