A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890925



Internal ID22665956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:189545889..189545939hg38UCSC Ensembl
chr2:190410615..190410665hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17398540
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890925
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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