A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084960



Internal ID21994193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46052033..46052033hg38UCSC Ensembl
chr13:46626168..46626168hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597884
Samples
Known GenesZC3H13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084960
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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