A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6080815



Internal ID21990048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73575141..73575141hg38UCSC Ensembl
chr13:74149278..74149278hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612650
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6080815
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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