A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5472069



Internal ID249789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:153246886..153247176hg38UCSC Ensembl
chr4:154168038..154168328hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16957128
Samples
Known GenesTRIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5472069
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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