A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17635545



Internal ID21827592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38945470..38945470hg38UCSC Ensembl
chr19:39436110..39436110hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107831
Supporting Variants
Samples
Known GenesFBXO17
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17635545
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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