A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537324



Internal ID20910662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47825284..47841417hg38UCSC Ensembl
chr22:48221033..48237166hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3816134
hg1916134
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205071
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537324
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