A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5957188



Internal ID22732328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:22929327..22929327hg38UCSC Ensembl
chr2:23152199..23152199hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17397445
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5957188
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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