A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011578



Internal ID22073209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:18134261..18335528hg38UCSC Ensembl
Outerchr16:18104860..18540265hg38UCSC Ensembl
Innerchr16:18228118..18429385hg19UCSC Ensembl
Outerchr16:18198717..18551587hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38435406
hg19352871
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155257
Supporting Variants
Samples
Known GenesLOC100288162, 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)nssv4011578
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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