A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745855



Internal ID20521866
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 StatusM
Merged Variants
Supporting Variantsnssv16266056
Samples
Known GenesTTBK2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745855
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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