A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5955251



Internal ID22730465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39209795..39209795hg38UCSC Ensembl
chr3:39251286..39251286hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410370
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5955251
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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