A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039014



Internal ID18781545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3965728..4070295hg38UCSC Ensembl
Innerchr16:4015729..4120296hg19UCSC Ensembl
Innerchr16:3955730..4060297hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38104568
hg19104568
hg18104568
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3556969
Samples
Known GenesADCY9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039014
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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