A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101449



Internal ID22010682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59410554..59410554hg38UCSC Ensembl
chr18:57077786..57077786hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17629053
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101449
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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