A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5960631



Internal ID22735603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122726893..122726893hg38UCSC Ensembl
chr3:122445740..122445740hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38412
hg19412
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397094
Samples
Known GenesPARP14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5960631
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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