A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095078



Internal ID22004311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106245709..106245709hg38UCSC Ensembl
chr13:106898058..106898058hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17615083
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095078
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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