A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062610



Internal ID21971843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38753905..38753905hg38UCSC Ensembl
chr8:38611423..38611423hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577048
Samples
Known GenesTACC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062610
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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