A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17373378



Internal ID22599047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11743367..11746953hg38UCSC Ensembl
chr16:11837223..11840809hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg383587
hg193587
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945268
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17373378
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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