A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622681



Internal ID21814728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13786913..13792472hg38UCSC Ensembl
chr19:13897727..13903286hg19UCSC Ensembl
Cytoband19p13.13
Allele length
AssemblyAllele length
hg385560
hg195560
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6050911
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622681
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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