A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958568



Internal ID22733630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19970178..19970244hg38UCSC Ensembl
chr22:19957701..19957767hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17394028
Samples
Known GenesARVCF
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958568
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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