A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538606



Internal ID20911919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50394699..50395830hg38UCSC Ensembl
chr20:49011236..49012367hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg381132
hg191132
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205272
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538606
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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