A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097595



Internal ID21273225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68553571..68590655hg38UCSC Ensembl
Innerchr17:66549712..66586796hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3837085
hg1937085
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113757
Supporting Variants
Samplessample189
Known GenesFAM20A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097595
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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