A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547598



Internal ID20920799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63914862..63926070hg38UCSC Ensembl
chr20:62546215..62557423hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3811209
hg1911209
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203443
Samples
Known GenesDNAJC5, MIR941-1, MIR941-2, MIR941-3, MIR941-4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547598
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