A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109809



Internal ID22019042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4189516..4189516hg38UCSC Ensembl
chr18:4189516..4189516hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628009
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109809
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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