A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418722



Internal ID21076275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69677693..69698823hg38UCSC Ensembl
chr8:70589928..70611058hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3821131
hg1921131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222683
Samples
Known GenesSLCO5A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418722
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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