A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100360



Internal ID21270805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20569799..20840374hg38UCSC Ensembl
Innerchr19:20752605..21023180hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38270576
hg19270576
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117158
Supporting Variants
Samplessample155
Known GenesZNF626
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100360
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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