A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3718892



Internal ID18670487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14658340..14958280hg38UCSC Ensembl
Innerchr16:14752197..15052137hg19UCSC Ensembl
Innerchr16:14659698..14959638hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38299941
hg19299941
hg18299941
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040576
Supporting Variants
Samples
Known GenesABCC6P2, BFAR, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO1, NPIPA1, NPIPA2, NPIPA3, PLA2G10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3718892
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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