A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517596



Internal ID20890957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35220286..35221339hg38UCSC Ensembl
chr20:33808089..33809142hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381054
hg191054
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203312
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517596
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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