A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6550580



Internal ID20923719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53362247..53421837hg38UCSC Ensembl
chr20:51978786..52038376hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3859591
hg1959591
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205879
Samples
Known GenesTSHZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6550580
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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