A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170036



Internal ID21314097
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14246665, nssv14242900
SamplesMLY_5, NGO_55
Known GenesMIR548AA2, MIR548D2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170036
Frequency
Sample Size93
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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