A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408118



Internal ID21065671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:18409586..18411518hg38UCSC Ensembl
chr6:18409817..18411749hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381933
hg191933
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228600
Samples
Known GenesRNF144B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408118
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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