A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6082227



Internal ID21991460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:94019923..94019923hg38UCSC Ensembl
chr15:94563152..94563152hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600756
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6082227
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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