A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760515



Internal ID20536375
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 StatusM
Merged Variants
Supporting Variantsnssv16262237
Samples
Known GenesFURIN
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760515
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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