A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3498n100



Internal ID22789585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:27257073..27596469hg38UCSC Ensembl
chr19:27747981..28087377hg19UCSC Ensembl
chr19:32439821..32779217hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38339397
hg19339397
hg18339397
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065696, nsv1066032, nsv1062077, nsv1065724
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)dgv3498n100
Frequency
Sample Size11257
Observed Gain18
Observed Loss11
Observed Complex0
Frequencyn/a


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