A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100463



Internal ID22009696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:41596782..41596782hg38UCSC Ensembl
chr18:39176746..39176746hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634707
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100463
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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