A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16948869



Internal ID33268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38797000..38828000hg38UCSC Ensembl
chr4:38798621..38829621hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3831001
hg1931001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466354
Supporting Variants
Samples
Known GenesTLR1, TLR6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16948869
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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