A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571534



Internal ID16012257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15386022..18005942hg38UCSC Ensembl
Innerchr16:15479879..18099799hg19UCSC Ensembl
Innerchr16:15387380..18007300hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg382619921
hg192619921
hg182619921
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4924n54
Supporting Variantsnssv852813
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)nsv571534
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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