A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530766



Internal ID20904127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35149225..35159585hg38UCSC Ensembl
chr20:33737028..33747388hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3810361
hg1910361
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203309
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530766
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer