A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097188



Internal ID21403052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51891711..51891711hg38UCSC Ensembl
chr15:52183908..52183908hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654076
Supporting Variants
SamplesHG00171
Known GenesTMOD3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097188
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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