A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2905n100



Internal ID22788992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:33024675..34208804hg38UCSC Ensembl
chr16:33035996..34011271hg19UCSC Ensembl
chr16:32943497..33918772hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381184130
hg19975276
hg18975276
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055989, nsv1066297, nsv1060755, nsv1060353
Samples
Known GenesLINC00273, LOC390705, RNU6-76P, TP53TG3, TP53TG3B, TP53TG3C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2905n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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