A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17119603



Internal ID21420774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45042625..45042695hg38UCSC Ensembl
chr21:46462540..46462610hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588726
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17119603
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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