A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17125620



Internal ID21497306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38340634..38341949hg38UCSC Ensembl
chr22:38736639..38737954hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381316
hg191316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593764
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17125620
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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