A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062102



Internal ID21971335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64643090..64643090hg38UCSC Ensembl
chr8:65555647..65555647hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583944
Samples
Known GenesCYP7B1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062102
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer