A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17609715



Internal ID21801762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90871538..90871538hg38UCSC Ensembl
chr15:91414768..91414768hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6084507
Supporting Variants
Samples
Known GenesFURIN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17609715
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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