A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884887



Internal ID22659871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21215450..21226145hg38UCSC Ensembl
chr2:21438322..21449017hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3810696
hg1910696
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17400659
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884887
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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