A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092233



Internal ID22001466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:48947592..48947592hg38UCSC Ensembl
chr13:49521728..49521728hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg382559
hg192559
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601985
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092233
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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