A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651854



Internal ID21600159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78397289..78397289hg38UCSC Ensembl
chr17:76393370..76393370hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092196
SamplesNA19239
Known GenesPGS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651854
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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