A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081520



Internal ID21990753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113913985..113913985hg38UCSC Ensembl
chr13:114616958..114616958hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607602
Samples
Known GenesLINC00452
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081520
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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