A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081536



Internal ID21990769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39030894..39030894hg38UCSC Ensembl
chr13:39605031..39605031hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612968
Samples
Known GenesPROSER1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081536
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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