A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086800



Internal ID21448457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71688304..71699209hg38UCSC Ensembl
chr15:71980643..71991548hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3810906
hg1910906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603779
Supporting Variants
SamplesHG00864
Known GenesTHSD4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086800
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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