A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669909



Internal ID21618214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49926623..49926623hg38UCSC Ensembl
chr22:50320271..50320271hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg382191
hg192191
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121927
SamplesNA19239
Known GenesCRELD2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669909
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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