A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103099



Internal ID22012332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3518189..3518189hg38UCSC Ensembl
chr19:3518187..3518187hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623710
Samples
Known GenesFZR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103099
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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