A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965876



Internal ID22740811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:5096175..5096279hg38UCSC Ensembl
chr21:45585537..45585641hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402638
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965876
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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