A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1782n100



Internal ID22787869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:19773626..19955201hg38UCSC Ensembl
chr14:20241785..20423360hg19UCSC Ensembl
chr14:19311625..19493200hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38181576
hg19181576
hg18181576
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054104, nsv1038557
Samples
Known GenesOR4K1, OR4K2, OR4K5, OR4M1, OR4N2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1782n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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