A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4441811



Internal ID22107992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17135754..17136070hg38UCSC Ensembl
chr22:17616644..17616960hg19UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15760606
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=DEL;REPTYPE=CONTRAC
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nsv4441811
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer