A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484667



Internal ID21142220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27209622..27517805hg38UCSC Ensembl
chr13:27783759..28091942hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38308184
hg19308184
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193589
Samples
Known GenesGTF3A, MTIF3, RASL11A, RPL21, RPL21P28, SNORA27, SNORD102
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484667
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