A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5441028



Internal ID219516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25054384..25060218hg38UCSC Ensembl
chr4:25056006..25061840hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg385835
hg195835
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16947023
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5441028
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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