A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2871n100



Internal ID22788958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:32369618..33829351hg38UCSC Ensembl
chr16:32380939..33631818hg19UCSC Ensembl
chr16:32288440..33539319hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381459734
hg191250880
hg181250880
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063831, nsv1062306, nsv1067059, nsv1056374, nsv1066244, nsv1060688, nsv1063293, nsv1057092, nsv1063452, nsv1056832, nsv1067115, nsv1067337, nsv1063358, nsv1061042, nsv1061801, nsv1061140, nsv1062026, nsv1057746, nsv1055882, nsv1057654, nsv1057268, nsv1062722, nsv1066937, nsv1058576, nsv1056873, nsv1060912, nsv1061610, nsv1063249, nsv1060660, nsv1067011
Samples
Known GenesLOC390705, 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)dgv2871n100
Frequency
Sample Size11257
Observed Gain58
Observed Loss0
Observed Complex0
Frequencyn/a


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