A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466492



Internal ID244327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:83610579..83619424hg38UCSC Ensembl
chr5:82906398..82915243hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg388846
hg198846
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16967108
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466492
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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