A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950634



Internal ID22726029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143920633..143920633hg38UCSC Ensembl
chr3:143639475..143639475hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397441
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950634
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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