A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065097



Internal ID21974330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26812993..26812993hg38UCSC Ensembl
chr8:26670510..26670510hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557911
Samples
Known GenesADRA1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065097
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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