A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465374



Internal ID243236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107041116..107042132hg38UCSC Ensembl
chr6:107362320..107363336hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381017
hg191017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986337
Samples
Known GenesC6orf203
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465374
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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