A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065671



Internal ID21974904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30043245..30043245hg38UCSC Ensembl
chr8:29900761..29900761hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065671
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