A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14246665



Internal ID21310106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:22706267..22779063hg38UCSC Ensembl
Outerchr16:22701658..22783408hg38UCSC Ensembl
Innerchr16:22717588..22790384hg19UCSC Ensembl
Outerchr16:22712979..22794729hg19UCSC Ensembl
Innerchr16:22625089..22697885hg18UCSC Ensembl
Outerchr16:22620480..22702230hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3881751
hg1981751
hg1881751
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170036
Supporting Variants
SamplesNGO_55
Known GenesMIR548AA2, MIR548D2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14246665
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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