A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17391714



Internal ID22449584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31673485..31673534hg38UCSC Ensembl
chr19:32164391..32164440hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944284
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17391714
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1.00


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