A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083306



Internal ID21992539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48136772..48136772hg38UCSC Ensembl
chr13:48710908..48710908hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605018
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083306
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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