A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068479



Internal ID21977712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80090094..80090094hg38UCSC Ensembl
chr8:81002329..81002329hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38808
hg19808
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597372
Samples
Known GenesTPD52
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068479
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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