A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259559



Internal ID20468777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43780529..43780529hg38UCSC Ensembl
chr19:44284681..44284681hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4761225
Supporting Variants
Samples
Known GenesKCNN4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259559
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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