A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586738



Internal ID21535294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:29455163..29457354hg38UCSC Ensembl
chr17:27782181..27784372hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg382192
hg192192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081098
SamplesNA19238
Known GenesTAOK1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586738
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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