A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5588734



Internal ID21537297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34905403..34918713hg38UCSC Ensembl
chr22:35301393..35314703hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3813311
hg1913311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137194
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5588734
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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