A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946035



Internal ID22721519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98151184..98152275hg38UCSC Ensembl
chr15:98694413..98695504hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381092
hg191092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384338
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946035
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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