A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084513



Internal ID21447159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47227947..47228016hg38UCSC Ensembl
chr15:47520144..47520213hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593836
Supporting Variants
SamplesHG00732
Known GenesSEMA6D
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084513
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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