A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1762n100



Internal ID19012130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:18605720..19906486hg38UCSC Ensembl
chr14:19382197..20374645hg19UCSC Ensembl
chr14:18452197..19444485hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381300767
hg19992449
hg18992289
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036313, nsv1035572, nsv1048880, nsv1053042, nsv1047744, nsv1045783, nsv1042633, nsv1045112, nsv1036687, nsv1039090, nsv1038682, nsv1050761, nsv1041099, nsv1046750, nsv1049199
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H2, OR4K2, OR4M1, OR4N2, OR4Q3, POTEG, POTEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1762n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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