A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087991



Internal ID21997224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113913797..113913797hg38UCSC Ensembl
chr13:114616770..114616770hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605294
Samples
Known GenesLINC00452
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087991
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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