A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456618



Internal ID234679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38799999..38801453hg38UCSC Ensembl
chr4:38801620..38803074hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381455
hg191455
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16948870
Samples
Known GenesTLR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456618
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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