A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220600



Internal ID22365253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:68630835..68631247hg38UCSC Ensembl
chr8:69543070..69543482hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14342415
SamplesHG00732
Known GenesC8orf34
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220600
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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