A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2854n100



Internal ID22788941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:32147274..33043325hg38UCSC Ensembl
chr16:32158595..33054646hg19UCSC Ensembl
chr16:32066096..32962147hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38896052
hg19896052
hg18896052
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057931, nsv1064815, nsv1065801, nsv1061591, nsv1059129, nsv1057587, nsv1064407, nsv1060871, nsv1064866, nsv1065879, nsv1066270, nsv1057138
Samples
Known GenesHERC2P4, LOC390705, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2854n100
Frequency
Sample Size11257
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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