A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758734



Internal ID20534594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169667687..169667687hg38UCSC Ensembl
chr4:170588838..170588838hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289514
Samples
Known GenesCLCN3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758734
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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