A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262237



Internal ID20471455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90871534..90871534hg38UCSC Ensembl
chr15:91414764..91414764hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4760515
Supporting Variants
Samples
Known GenesFURIN
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262237
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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