A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17620274



Internal ID21812321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38810642..38810642hg38UCSC Ensembl
chr19:39301282..39301282hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6101177
Supporting Variants
Samples
Known GenesLGALS4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17620274
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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