A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2898n100



Internal ID22788985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:32732148..34176379hg38UCSC Ensembl
chr16:32743469..33978846hg19UCSC Ensembl
chr16:32650970..33886347hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381444232
hg191235378
hg181235378
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063749, nsv1064889, nsv1058089, nsv1064084, nsv1061411, nsv1063162, nsv1066571, nsv1066620, nsv1065454, nsv1058281, nsv1055664, nsv1062978, nsv1062397, nsv1063486
Samples
Known GenesLINC00273, LOC390705, RNU6-76P, SLC6A10P, 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)dgv2898n100
Frequency
Sample Size11257
Observed Gain21
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer