A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980564



Internal ID21889907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1053199..1053252hg38UCSC Ensembl
chr1:988579..988632hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17525911
Samples
Known GenesAGRN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980564
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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