A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3928711



Internal ID21348781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90871538..90871538hg38UCSC Ensembl
chr15:91414768..91414768hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15195437
SamplesHG002
Known GenesFURIN
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3928711
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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