A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535514



Internal ID20908875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35935264..35954972hg38UCSC Ensembl
chr20:34523186..34542894hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3819709
hg1919709
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202209
Samples
Known GenesPHF20, SCAND1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535514
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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