A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518308



Internal ID20891669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34538206..34545408hg38UCSC Ensembl
chr20:33126010..33133212hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg387203
hg197203
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203306
Samples
Known GenesDYNLRB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518308
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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