A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518704



Internal ID20892065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33314253..33321156hg38UCSC Ensembl
chr20:31902059..31908962hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg386904
hg196904
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203285
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518704
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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