A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699980



Internal ID123646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24889551..24901361hg38UCSC Ensembl
chr15:25134698..25146508hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3811811
hg1911811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5495647
Supporting Variants
Samples
Known GenesSNRPN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699980
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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