A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460866



Internal ID238836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4086302..4090342hg38UCSC Ensembl
chr6:4086536..4090576hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg384041
hg194041
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979910
Samples
Known GenesC6orf201
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460866
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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