A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493574



Internal ID21151127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:21448801..21459300hg38UCSC Ensembl
chr13:22022940..22033439hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3810500
hg1910500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192487
Samples
Known GenesZDHHC20
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493574
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