A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265891



Internal ID20475109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:17163445..17163561hg38UCSC Ensembl
chr3:17204937..17205053hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730983
Supporting Variants
Samples
Known GenesTBC1D5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265891
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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