A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5940814



Internal ID22716228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:53349952..53350028hg38UCSC Ensembl
chr15:53642149..53642225hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389003
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5940814
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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