A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528627



Internal ID20901988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2737170..2779572hg38UCSC Ensembl
chr20:2717816..2760218hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3842403
hg1942403
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202568
Samples
Known GenesEBF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528627
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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