A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111244



Internal ID22020477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18206129..18206129hg38UCSC Ensembl
chr19:18316939..18316939hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621861
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111244
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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