A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938452



Internal ID22713832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26316126..26336881hg38UCSC Ensembl
chr15:26561273..26582028hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3820756
hg1920756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370716
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938452
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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