A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17390220



Internal ID22448090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14020508..14029364hg38UCSC Ensembl
chr3:14062008..14070864hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg388857
hg198857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901344
Supporting Variants
Samples
Known GenesTPRXL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17390220
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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