A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610837



Internal ID21802884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67083177..67084709hg38UCSC Ensembl
chr15:67375515..67377047hg19UCSC Ensembl
Cytoband15q22.33
Allele length
AssemblyAllele length
hg381533
hg191533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6031706
Supporting Variants
Samples
Known GenesSMAD3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610837
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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