A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466512



Internal ID244346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:25125113..25125453hg38UCSC Ensembl
chr5:25125222..25125562hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16965207
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466512
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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