A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17397582



Internal ID22455452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:28304081..28469209hg38UCSC Ensembl
chr21:29676400..29841530hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38165129
hg19165131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5962423
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17397582
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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