A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109668



Internal ID22018901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1967717..1967717hg38UCSC Ensembl
chr19:1967716..1967716hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617946
Samples
Known GenesCSNK1G2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109668
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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