A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641743



Internal ID21590048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177506687..177506687hg38UCSC Ensembl
chr5:176933688..176933688hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128851
SamplesNA19650
Known GenesDOK3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641743
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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