A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405158



Internal ID21062711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49467101..49471200hg38UCSC Ensembl
chr6:49434814..49438913hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236812
Samples
Known GenesCENPQ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405158
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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