A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941616



Internal ID22717043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36083984..36190304hg38UCSC Ensembl
chr17:34411341..34517693hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38106321
hg19106353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv911n209
Supporting Variantsnssv17387698
Samples
Known GenesCCL3, CCL4, TBC1D3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941616
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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