A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735921



Internal ID20511864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165039510..165039832hg38UCSC Ensembl
chr4:165960662..165960984hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288966
Samples
Known GenesTRIM60
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735921
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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