A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412087



Internal ID21069640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21831115..21835541hg38UCSC Ensembl
chr6:21831346..21835772hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384427
hg194427
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220635
Samples
Known GenesCASC15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412087
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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