A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17593260



Internal ID21785303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103320133..103320133hg38UCSC Ensembl
chr8:104332361..104332361hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6074881
Supporting Variants
Samples
Known GenesFZD6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17593260
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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