A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069387



Internal ID21978620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40374044..40374044hg38UCSC Ensembl
chr8:40231563..40231563hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590413
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069387
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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