A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469889



Internal ID247664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18319500..18321958hg38UCSC Ensembl
chr6:18319731..18322189hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382459
hg192459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16981171
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469889
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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