A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5470208



Internal ID247977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139236705..139240803hg38UCSC Ensembl
chr4:140157859..140161957hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg384099
hg194099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735173
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5470208
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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