A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4737334



Internal ID20513294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23451159..23455598hg38UCSC Ensembl
chr3:23492650..23497089hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg384440
hg194440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276987
Samples
Known GenesMIR548AC, UBE2E2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4737334
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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