A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525013



Internal ID20898374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34242485..34245641hg38UCSC Ensembl
chr20:32830291..32833447hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg383157
hg193157
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203301
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525013
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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