A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv490n100



Internal ID22786577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:189255731..189645524hg38UCSC Ensembl
chr1:189224862..189614654hg19UCSC Ensembl
chr1:187491485..187881277hg18UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38389794
hg19389793
hg18389793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009494, nsv1014923, nsv1006590
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv490n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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