A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17593856



Internal ID21785899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65429328..65436303hg38UCSC Ensembl
chr8:66341563..66348538hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg386976
hg196976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6010239
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17593856
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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