A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284289



Internal ID20493507
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 StatusS
Merged Variantsnsv4746373
Supporting Variants
Samples
Known GenesTACR3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284289
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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