A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080488



Internal ID21403755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69122453..69122453hg38UCSC Ensembl
chr15:69414792..69414792hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5657483
Supporting Variants
SamplesHG00171
Known GenesMIR548H4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080488
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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