A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17627611



Internal ID21819658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18441993..18442626hg38UCSC Ensembl
chr19:18552803..18553436hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6059699
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17627611
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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