A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372340



Internal ID22598009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67115604..67115661hg38UCSC Ensembl
chr15:67407942..67407999hg19UCSC Ensembl
Cytoband15q22.33
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5947349
Supporting Variants
Samples
Known GenesSMAD3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372340
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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