A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2767n100



Internal ID20154383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14959856..15014718hg38UCSC Ensembl
chr16:15053713..15108575hg19UCSC Ensembl
chr16:14961214..15016076hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3854863
hg1954863
hg1854863
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1042555, nsv1037702
Samples
Known GenesMIR1972-1, MIR1972-2, PDXDC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2767n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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