A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5453155



Internal ID231289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:12559972..12722033hg38UCSC Ensembl
chr4:12561596..12723657hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38162062
hg19162062
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16947769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5453155
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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