A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981917



Internal ID21891260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:166046721..166046773hg38UCSC Ensembl
chr1:166015958..166016010hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17525213
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981917
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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