A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657533



Internal ID21605838
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 StatusM
Merged Variants
Supporting Variantsnssv17082037
SamplesHG00512
Known GenesTHSD4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657533
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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