A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467259



Internal ID245078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19865086..19867273hg38UCSC Ensembl
chr6:19865317..19867504hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382188
hg192188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979276
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467259
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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