A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1761n100



Internal ID22787848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:18605720..19799717hg38UCSC Ensembl
chr14:19382197..20267876hg19UCSC Ensembl
chr14:18452197..19337716hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381193998
hg19885680
hg18885520
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052317, nsv1042377, nsv1040110, nsv1054743, nsv1046328, nsv1043361, nsv1040783
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H2, OR4M1, 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)dgv1761n100
Frequency
Sample Size11257
Observed Gain8
Observed Loss12
Observed Complex0
Frequencyn/a


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