A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5617642



Internal ID21565947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122726893..122726893hg38UCSC Ensembl
chr3:122445740..122445740hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127564
SamplesHG00512
Known GenesPARP14
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5617642
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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