A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266056



Internal ID20475274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42801159..42801315hg38UCSC Ensembl
chr15:43093357..43093513hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745855
Supporting Variants
Samples
Known GenesTTBK2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266056
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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