A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074881



Internal ID21984114
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 StatusM
Merged Variants
Supporting Variantsnssv17593260
Samples
Known GenesFZD6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074881
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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