A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372483



Internal ID22598152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68027534..68028704hg38UCSC Ensembl
chr15:68319872..68321042hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381171
hg191171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5930840
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372483
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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