A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203277



Internal ID20770317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32701117..32769216hg38UCSC Ensembl
chr20:31288919..31357022hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3868100
hg1968104
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529985
Supporting Variants
Samples
Known GenesCOMMD7, DNMT3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203277
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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