A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5119n100



Internal ID20156735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:9804044..9895896hg38UCSC Ensembl
chr4:9805668..9897520hg19UCSC Ensembl
chr4:9414766..9506618hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3891853
hg1991853
hg1891853
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1001175, nsv1001832
Samples
Known GenesSLC2A9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5119n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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