A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540468



Internal ID20913760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56732791..56736141hg38UCSC Ensembl
chr20:55307847..55311197hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg383351
hg193351
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203896
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540468
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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