A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958156



Internal ID39419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153684874..153684883hg38UCSC Ensembl
chr4:154606026..154606035hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534003
Supporting Variants
Samples
Known GenesTLR2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958156
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00562


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