A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618315



Internal ID21810362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10213358..10218044hg38UCSC Ensembl
chr19:10324034..10328720hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg384687
hg194687
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6053969
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618315
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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