A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947393



Internal ID22722898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89315512..89315591hg38UCSC Ensembl
chr15:89858743..89858822hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384754
Samples
Known GenesFANCI
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947393
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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