A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5958209



Internal ID22733285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:23104144..23104144hg38UCSC Ensembl
chr2:23327015..23327015hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17403355
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5958209
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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