A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334965



Internal ID20868155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206634201..206638300hg38UCSC Ensembl
chr1:206807546..206811645hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199886
Samples
Known GenesDYRK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334965
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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