A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533140



Internal ID20906501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11881901..11894600hg38UCSC Ensembl
chr20:11862549..11875248hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3812700
hg1912700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202163
Samples
Known GenesBTBD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533140
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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