A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1764n100



Internal ID19012132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:18976182..19886834hg38UCSC Ensembl
chr14:19562127..20354993hg19UCSC Ensembl
chr14:18632127..19424833hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38910653
hg19792867
hg18792707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045226, nsv1037871, nsv1051258, nsv1043167, nsv1038708, nsv1038259, nsv1035585, nsv1054493, nsv1052102, nsv1037495, nsv1039954, nsv1041471, nsv1039634, nsv1049928, nsv1043756, nsv1039208, nsv1039321, nsv1041540, nsv1040034, nsv1041655, nsv1047024, nsv1048490, nsv1042558, nsv1044880, nsv1043742, nsv1047613, nsv1042240, nsv1054677, nsv1042476, nsv1053473, nsv1040894
Samples
Known GenesBMS1P17, BMS1P18, 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)dgv1764n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss45
Observed Complex0
Frequencyn/a


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