A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755903



Internal ID20531763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51891717..51891717hg38UCSC Ensembl
chr15:52183914..52183914hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270794
Samples
Known GenesTMOD3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755903
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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