A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980516



Internal ID21889859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109724414..109724643hg38UCSC Ensembl
chr1:110267036..110267265hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532162
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980516
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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