A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112107



Internal ID22021341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:60696049..60696049hg38UCSC Ensembl
chr18:58363282..58363282hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17636450
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112107
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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