A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17118513



Internal ID21506538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33175111..33175111hg38UCSC Ensembl
chr21:34547416..34547416hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670954
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17118513
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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