A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027309



Internal ID21936652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20228766..20260684hg38UCSC Ensembl
chr13:20802905..20834823hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3831919
hg1931919
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600546
Samples
Known GenesGJB6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027309
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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