A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459014



Internal ID237033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95705807..95713807hg38UCSC Ensembl
chr5:95041511..95049511hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg388001
hg198001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16970628
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459014
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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