A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067284



Internal ID19156503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32102349..32473866hg38UCSC Ensembl
Innerchr16:32113670..32485187hg19UCSC Ensembl
Innerchr16:32021171..32392688hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38371518
hg19371518
hg18371518
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2845n100
Supporting Variantsnssv3550250
Samples
Known GenesHERC2P4, LOC390705, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067284
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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