A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082037



Internal ID21405071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71199893..71199893hg38UCSC Ensembl
chr15:71492232..71492232hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5657533
Supporting Variants
SamplesHG00512
Known GenesTHSD4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082037
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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