A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3493n100



Internal ID22789580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:27257073..27294573hg38UCSC Ensembl
chr19:27747981..27785481hg19UCSC Ensembl
chr19:32439821..32477321hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg3837501
hg1937501
hg1837501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061063, nsv1055949
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)dgv3493n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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