A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5590799



Internal ID21539369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39357599..39357660hg38UCSC Ensembl
chr22:39753604..39753665hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131691
SamplesHG00731
Known GenesSYNGR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5590799
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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