A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941658



Internal ID22717086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69451991..69452334hg38UCSC Ensembl
chr15:69744330..69744673hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385572
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941658
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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