A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6064n223



Internal ID22809032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15146133..15160135hg38UCSC Ensembl
chr6:15146364..15160366hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3814003
hg1914003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6407386, nsv6399031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6064n223
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