A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068797



Internal ID21978030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123382681..123382681hg38UCSC Ensembl
chr8:124394921..124394921hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580211
Samples
Known GenesATAD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068797
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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