A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5952775



Internal ID22728079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:5098516..5098570hg38UCSC Ensembl
chr21:45583233..45583342hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3855
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401367
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5952775
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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