A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746373



Internal ID20522386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103650667..103650869hg38UCSC Ensembl
chr4:104571824..104572026hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284289
Samples
Known GenesTACR3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746373
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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