A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004926



Internal ID21914269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100674448..100677176hg38UCSC Ensembl
chr8:101686676..101689404hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg382729
hg192729
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588673
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004926
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