A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3084n100



Internal ID20154700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3045742..3209683hg38UCSC Ensembl
chr17:2949036..3112977hg19UCSC Ensembl
chr17:2895786..3059727hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38163942
hg19163942
hg18163942
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056009, nsv1060727
Samples
Known GenesOR1A2, OR1D2, OR1D5, OR1G1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3084n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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