A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2763n100



Internal ID20154379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14954899..15031584hg38UCSC Ensembl
chr16:15048756..15125441hg19UCSC Ensembl
chr16:14956257..15032942hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3876686
hg1976686
hg1876686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054479, nsv1054248, nsv1040581, nsv1054771, nsv1046771, nsv1037379, nsv1042379, nsv1048565, nsv1047003, nsv1046810
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)dgv2763n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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