A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087343



Internal ID21996576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109365902..109365902hg38UCSC Ensembl
chr13:110018249..110018249hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600884
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087343
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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