A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965858



Internal ID22740793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10690415..10690415hg38UCSC Ensembl
chr2:10830541..10830541hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397932
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965858
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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