A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1755n100



Internal ID22787842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:18497136..19350746hg38UCSC Ensembl
chr14:19273613..19938429hg19UCSC Ensembl
chr14:18343613..19008429hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38853611
hg19664817
hg18664817
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053054, nsv1036949, nsv1043334, nsv1044317, nsv1036252, nsv1051852
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H12, POTEG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1755n100
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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