A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1771n100



Internal ID19012139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19256386..19842764hg38UCSC Ensembl
chr14:19844095..20310923hg19UCSC Ensembl
chr14:18914095..19380763hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38586379
hg19466829
hg18466669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050159, nsv1039648, nsv1041113, nsv1050187, nsv1039945, nsv1048210, nsv1041079, nsv1042435, nsv1039722, nsv1044981
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, 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)dgv1771n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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