A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852814



Internal ID15800084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15386022..18071186hg38UCSC Ensembl
Innerchr16:15479879..18165043hg19UCSC Ensembl
Innerchr16:15387380..18072544hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg382685165
hg192685165
hg182685165
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571535
Supporting Variants
Samples
Known GenesABCC1, ABCC6, C16orf45, FOPNL, KIAA0430, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR484, MIR6506, MIR6511A-2, MIR6770-2, MPV17L, MYH11, NDE1, NOMO3, NPIPA7, NPIPA8, PKD1P1, XYLT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852814
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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