A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5468940



Internal ID246733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16178603..16189491hg38UCSC Ensembl
chr6:16178834..16189722hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3810889
hg1910889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979090
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5468940
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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