A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17118854



Internal ID21404069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:28673396..28673653hg38UCSC Ensembl
chr21:30045718..30045975hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593246
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17118854
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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