A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3558029



Internal ID18509624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:16283793..16695080hg38UCSC Ensembl
Innerchr16:16377650..16788937hg19UCSC Ensembl
Innerchr16:16285151..16696438hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38411288
hg19411288
hg18411288
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050063
Supporting Variants
Samples
Known GenesLOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO3, NPIPA7, NPIPA8, PKD1P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3558029
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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