A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701202



Internal ID124868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47372267..47395405hg38UCSC Ensembl
chr15:47664464..47687602hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3823139
hg1923139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5514065
Supporting Variants
Samples
Known GenesSEMA6D
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701202
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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