A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594472



Internal ID21786515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109778677..109779217hg38UCSC Ensembl
chr8:110790906..110791446hg19UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6006348
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594472
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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