A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17535683



Internal ID21860038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:25730474..25730474hg38UCSC Ensembl
chr2:25953343..25953343hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6048143
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17535683
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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