A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093916



Internal ID22003149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108258223..108258223hg38UCSC Ensembl
chr13:108910571..108910571hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602867
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093916
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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