A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965104



Internal ID22740039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102798276..102798276hg38UCSC Ensembl
chr4:103719433..103719433hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411619
Samples
Known GenesUBE2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965104
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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