A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660866



Internal ID21609171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8226645..8226645hg38UCSC Ensembl
chr17:8129963..8129963hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092131
SamplesNA19983
Known GenesCTC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660866
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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