A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542900



Internal ID20916151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32653710..32661589hg38UCSC Ensembl
chr22:33049696..33057575hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg387880
hg197880
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204567
Samples
Known GenesSYN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542900
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