A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743199



Internal ID20519186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23871722..23872942hg38UCSC Ensembl
chr3:23913213..23914433hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg381221
hg191221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16265288
Samples
Known GenesUBE2E1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743199
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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