A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095288



Internal ID22004521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45713281..45713281hg38UCSC Ensembl
chr15:46005479..46005479hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602324
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095288
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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