A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940981



Internal ID22716397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42539368..42540085hg38UCSC Ensembl
chr15:42831566..42832283hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38718
hg19718
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376971
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940981
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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