A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027694



Internal ID21937037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113382333..113435382hg38UCSC Ensembl
chr13:114036648..114089697hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3853050
hg1953050
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607029
Samples
Known GenesADPRHL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027694
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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