A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17124659



Internal ID21454884
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 StatusS
Merged Variantsnsv5634471
Supporting Variants
SamplesHG02011
Known GenesDDX60
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17124659
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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