A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539408



Internal ID20912703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44230555..44231066hg38UCSC Ensembl
chr22:44626435..44626946hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207546
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539408
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