A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111113



Internal ID22020346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3442045..3442045hg38UCSC Ensembl
chr18:3442043..3442043hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634117
Samples
Known GenesTGIF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111113
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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