A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6098116



Internal ID22007349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78226793..78226793hg38UCSC Ensembl
chr15:78519135..78519135hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601232
Samples
Known GenesACSBG1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6098116
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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