A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928591



Internal ID22703833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65300776..65300932hg38UCSC Ensembl
chr15:65593114..65593270hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17382479
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928591
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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