A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3716921



Internal ID18668516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:18284986..18730776hg38UCSC Ensembl
Innerchr16:18378843..18742098hg19UCSC Ensembl
Innerchr16:18286344..18649599hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38445791
hg19363256
hg18363256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039416
Supporting Variants
Samples
Known GenesABCC6P1, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO2, NPIPA7, NPIPA8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3716921
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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