A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620347



Internal ID21812394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11425063..11425063hg38UCSC Ensembl
chr19:11535960..11535960hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107720
Supporting Variants
Samples
Known GenesCCDC151
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620347
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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