A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981608



Internal ID21890951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151022108..151022421hg38UCSC Ensembl
chr1:150994584..150994897hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531195
Samples
Known GenesPRUNE
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981608
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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