A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702288



Internal ID125954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85808038..85848378hg38UCSC Ensembl
chr15:86351269..86391609hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3840341
hg1940341
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5514644
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702288
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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