A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17562874



Internal ID21887229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28566826..28566826hg38UCSC Ensembl
chr8:28424343..28424343hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg382586
hg192586
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6061034
Supporting Variants
Samples
Known GenesFZD3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17562874
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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