A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3009n223



Internal ID22805977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15729576..15773940hg38UCSC Ensembl
chr17:15632890..15677254hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3844365
hg1944365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6499815, nsv6511228
Samples
Known GenesCDRT15P2, TBC1D26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3009n223
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