A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103420



Internal ID22012655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16487323..16487323hg38UCSC Ensembl
chr19:16598134..16598134hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381373
hg191373
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620174
Samples
Known GenesCALR3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103420
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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