A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935640



Internal ID22710984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47012294..47012443hg38UCSC Ensembl
chr15:47304492..47304641hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374373
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935640
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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