A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752375



Internal ID20528235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169945793..169945793hg38UCSC Ensembl
chr4:170866944..170866944hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270877
Samples
Known GenesLOC100506085
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752375
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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