A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17703940



Internal ID127606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69100854..69104952hg38UCSC Ensembl
chr15:69393194..69397292hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg384099
hg194099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521286
Supporting Variants
Samples
Known GenesMIR548H4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17703940
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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