A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979733



Internal ID22754668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80204170..80204170hg38UCSC Ensembl
chr15:80496512..80496512hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388231
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979733
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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