A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17118566



Internal ID21447718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36303812..36304045hg38UCSC Ensembl
chr21:37676110..37676343hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597616
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17118566
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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