A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17118654



Internal ID21461765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43335983..43336351hg38UCSC Ensembl
chr21:44755863..44756231hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588615
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17118654
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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