A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588883



Internal ID21780926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93039431..93039431hg38UCSC Ensembl
chr8:94051659..94051659hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080134
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588883
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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