A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702228



Internal ID125894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84931125..84941373hg38UCSC Ensembl
chr15:85474356..85484604hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3810249
hg1910249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5533735
Supporting Variants
Samples
Known GenesSLC28A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702228
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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