A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529131



Internal ID20902492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4730478..4751552hg38UCSC Ensembl
chr20:4711124..4732198hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3821075
hg1921075
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202920
Samples
Known GenesPRNT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529131
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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