A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv911n209



Internal ID22826986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36083984..36190322hg38UCSC Ensembl
chr17:34411341..34517711hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38106339
hg19106371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5943104, nsv5941616
Samples
Known GenesCCL3, CCL4, TBC1D3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv911n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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