A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834941



Internal ID22609876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13987924..13992360hg38UCSC Ensembl
chr3:14029424..14033860hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg384437
hg194437
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485172
Samples
Known GenesTPRXL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834941
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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