A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082091



Internal ID21991324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109654975..109654975hg38UCSC Ensembl
chr13:110307322..110307322hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613034
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082091
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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