A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702908



Internal ID126574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67145757..67145843hg38UCSC Ensembl
chr15:67438095..67438181hg19UCSC Ensembl
Cytoband15q22.33
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5529220
Supporting Variants
Samples
Known GenesSMAD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702908
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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