A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102198



Internal ID22011433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43617539..43617539hg38UCSC Ensembl
chr19:44121691..44121691hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628727
Samples
Known GenesZNF428
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102198
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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