A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3067n100



Internal ID20154683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:90013735..90221115hg38UCSC Ensembl
chr16:90080143..90287523hg19UCSC Ensembl
chr16:88607644..88815024hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38207381
hg19207381
hg18207381
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065796, nsv1063340, nsv1058809, nsv1066160, nsv1057294, nsv1060538, nsv1057794
Samples
Known GenesC16orf3, DBNDD1, GAS8, PRDM7, URAHP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3067n100
Frequency
Sample Size29084
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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