A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636031



Internal ID21828078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6280507..6289405hg38UCSC Ensembl
chr19:6280518..6289416hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg388899
hg198899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6056826
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636031
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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