A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5462178



Internal ID240112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42090781..42092813hg38UCSC Ensembl
chr4:42092798..42094830hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg382033
hg192033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16949610
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5462178
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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