A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541586



Internal ID20914868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37904165..37911779hg38UCSC Ensembl
chr22:38300172..38307786hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg387615
hg197615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204640
Samples
Known GenesMICALL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541586
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