A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111746



Internal ID22020979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15945737..15945737hg38UCSC Ensembl
chr19:16056547..16056547hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111746
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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