A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7685n223



Internal ID22810653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30622297..30751535hg38UCSC Ensembl
chr9:30622295..30751533hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38129239
hg19129239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6428340, nsv6422777
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7685n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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