A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011581



Internal ID22073212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:18191217..18737254hg38UCSC Ensembl
Outerchr16:18172683..18749771hg38UCSC Ensembl
Innerchr16:18285074..18748576hg19UCSC Ensembl
Outerchr16:18266540..18761093hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38577089
hg19494554
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155260
Supporting Variants
Samples
Known GenesABCC6P1, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO2, NPIPA7, NPIPA8
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011581
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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