A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5595730



Internal ID21544337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:23234669..23235624hg38UCSC Ensembl
chr22:23576856..23577811hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38956
hg19956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125577
SamplesHG03683
Known GenesBCR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5595730
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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