A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636464



Internal ID21828511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8352728..8359138hg38UCSC Ensembl
chr19:8417612..8424022hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg386411
hg196411
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042624
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17636464
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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