A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532928



Internal ID20906289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35722276..35724260hg38UCSC Ensembl
chr20:34310198..34312182hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381985
hg191985
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203319
Samples
Known GenesRBM39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532928
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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