A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076349



Internal ID21985582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10674282..10674282hg38UCSC Ensembl
chr8:10531792..10531792hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565545
Samples
Known GenesC8orf74
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076349
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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