A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078291



Internal ID21987524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:12873386..12873386hg38UCSC Ensembl
chr8:12730895..12730895hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559431
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078291
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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