A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6976n223



Internal ID22809944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81169833..81179722hg38UCSC Ensembl
chr7:80799149..80809038hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg389890
hg199890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6611549, nsv6607549
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6976n223
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