A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17387698



Internal ID22445568
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 StatusS
Merged Variantsnsv5941616
Supporting Variants
Samples
Known GenesCCL3, CCL4, TBC1D3B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17387698
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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