A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5983094



Internal ID21892437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234875799..234876004hg38UCSC Ensembl
chr1:235011546..235011751hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524272
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5983094
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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