A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4764289



Internal ID20540149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185827299..185827299hg38UCSC Ensembl
chr4:186748453..186748453hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259670
Samples
Known GenesSORBS2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4764289
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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