A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455514



Internal ID233593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38795944..38796746hg38UCSC Ensembl
chr4:38797565..38798367hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38803
hg19803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16948868
Samples
Known GenesTLR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455514
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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