A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036394



Internal ID21945737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:92046053..92489598hg38UCSC Ensembl
chr13:92698306..93141851hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38443546
hg19443546
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17614623
Samples
Known GenesGPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036394
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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