A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875215



Internal ID22650172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:223143029..223143166hg38UCSC Ensembl
chr1:223316371..223316508hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353499
Samples
Known GenesTLR5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875215
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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