A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081294



Internal ID21990527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80715110..80715110hg38UCSC Ensembl
chr15:81007451..81007451hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604752
Samples
Known GenesABHD17C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081294
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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