A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5648627



Internal ID21596932
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 Variantsnssv17084933
SamplesHG00731
Known GenesFURIN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5648627
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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