A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467898



Internal ID245708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151466109..151474055hg38UCSC Ensembl
chr6:151787244..151795190hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg387947
hg197947
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16989356
Samples
Known GenesC6orf211
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467898
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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