A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1767n100



Internal ID22787854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19230949..19922383hg38UCSC Ensembl
chr14:19790343..20390542hg19UCSC Ensembl
chr14:18860343..19460382hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38691435
hg19600200
hg18600040
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046676, nsv1036961, nsv1053049, nsv1041527, nsv1037316, nsv1039993, nsv1036212, nsv1040815, nsv1043617, nsv1051911, nsv1054928, nsv1054350, nsv1046272, nsv1045406, nsv1037094, nsv1044000, nsv1046179, nsv1041089, nsv1049925, nsv1042440, nsv1052324, nsv1043310, nsv1043505
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3, POTEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1767n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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