A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954545



Internal ID22729780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:30264385..30266275hg38UCSC Ensembl
chr21:31636703..31638593hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg381891
hg191891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405370
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5954545
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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