A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553157



Internal ID20926266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50241473..50241901hg38UCSC Ensembl
chr20:48858010..48858438hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205271
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553157
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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