A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068052



Internal ID21977285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34262069..34262069hg38UCSC Ensembl
chr8:34119587..34119587hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38409
hg19409
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557596
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068052
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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