A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589810



Internal ID21781853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47117787..47133124hg38UCSC Ensembl
chr8:48029410..48044747hg19UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg3815338
hg1915338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6001366
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589810
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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