A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3059n100



Internal ID20154675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85068826..85219999hg38UCSC Ensembl
chr16:85102432..85253605hg19UCSC Ensembl
chr16:83659933..83811106hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38151174
hg19151174
hg18151174
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058234, nsv1063064
Samples
Known GenesFAM92B, KIAA0513, LOC400548
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3059n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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