A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411185



Internal ID21068738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49460501..49466400hg38UCSC Ensembl
chr6:49428214..49434113hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220957
Samples
Known GenesCENPQ, MUT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411185
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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