A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551228



Internal ID20924365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62166601..62170600hg38UCSC Ensembl
chr20:60741657..60745656hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203407
Samples
Known GenesSS18L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551228
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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