A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525399



Internal ID20898760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39253124..39256301hg38UCSC Ensembl
chr20:37881767..37884944hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg383178
hg193178
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202254
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525399
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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