A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433051



Internal ID21395053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224059327..224059807hg38UCSC Ensembl
chr1:224247029..224247509hg19UCSC Ensembl
Cytoband1q42.11
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv50n172
Supporting Variantsnssv15750754
SamplesMDQ045
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433051
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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