A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933437



Internal ID22708750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:19793146..19835751hg38UCSC Ensembl
chr15:20000001..20041004hg19UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3842606
hg1941004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378304
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933437
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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