A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14242900



Internal ID21303225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:22706267..22770649hg38UCSC Ensembl
Outerchr16:22701658..22772270hg38UCSC Ensembl
Innerchr16:22717588..22781970hg19UCSC Ensembl
Outerchr16:22712979..22783591hg19UCSC Ensembl
Innerchr16:22625089..22689471hg18UCSC Ensembl
Outerchr16:22620480..22691092hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3870613
hg1970613
hg1870613
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170036
Supporting Variants
SamplesMLY_5
Known GenesMIR548AA2, MIR548D2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14242900
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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