A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091652



Internal ID22000885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78599765..78599765hg38UCSC Ensembl
chr15:78892107..78892107hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38771
hg19771
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611858
Samples
Known GenesCHRNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091652
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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