A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893317



Internal ID22668376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186081212..186082167hg38UCSC Ensembl
chr4:187002366..187003321hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38956
hg19956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417325
Samples
Known GenesTLR3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893317
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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