A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701633



Internal ID125299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44859031..45026043hg38UCSC Ensembl
chr15:45151229..45318241hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38167013
hg19167013
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562309
Supporting Variants
Samples
Known GenesC15orf43, SORD
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701633
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001717


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