A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17119281



Internal ID21506712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:30264385..30266275hg38UCSC Ensembl
chr21:31636703..31638593hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg381891
hg191891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591712
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17119281
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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