A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945441



Internal ID22720919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92146867..92147087hg38UCSC Ensembl
chr15:92690097..92690317hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373017
Samples
Known GenesSLCO3A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945441
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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