A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17127099



Internal ID21511474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21715659..21715840hg38UCSC Ensembl
chr22:22069948..22070129hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599125
Supporting Variants
SamplesNA24385
Known GenesYPEL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17127099
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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