A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467082



Internal ID244903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170223947..170228374hg38UCSC Ensembl
chr4:171145098..171149525hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg384428
hg194428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16960100
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467082
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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