A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5468660



Internal ID246456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:106468291..106627630hg38UCSC Ensembl
chr5:105803992..105963331hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg38159340
hg19159340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16971832
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5468660
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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