A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081098



Internal ID21490261
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 StatusS
Merged Variantsnsv5586738
Supporting Variants
SamplesNA19238
Known GenesTAOK1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081098
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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