A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110239



Internal ID22019472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44490060..44490060hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3857
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17625527
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110239
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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