A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5634471



Internal ID21582776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168297382..168297382hg38UCSC Ensembl
chr4:169218533..169218533hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124659
SamplesHG02011
Known GenesDDX60
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5634471
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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