A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959856



Internal ID22734875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21951192..21951423hg38UCSC Ensembl
chr22:22305564..22305795hg19UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401521
Samples
Known GenesPPM1F
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959856
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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