A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517458



Internal ID20890819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35166772..35176647hg38UCSC Ensembl
chr20:33754575..33764450hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg389876
hg199876
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203310
Samples
Known GenesPROCR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517458
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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