A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3497n100



Internal ID22789584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:27257073..27589895hg38UCSC Ensembl
chr19:27747981..28080803hg19UCSC Ensembl
chr19:32439821..32772643hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38332823
hg19332823
hg18332823
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065571, nsv1063001, nsv1066189, nsv1055959, nsv1062357, nsv1065098, nsv1065117, nsv1062651, nsv1059313, nsv1057310, nsv1057162, nsv1065405
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)dgv3497n100
Frequency
Sample Size11257
Observed Gain36
Observed Loss0
Observed Complex0
Frequencyn/a


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