A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3502n100



Internal ID22789589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:27260755..27590467hg38UCSC Ensembl
chr19:27751663..28081375hg19UCSC Ensembl
chr19:32443503..32773215hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38329713
hg19329713
hg18329713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063700, nsv1057937, nsv1065836, nsv1062502, nsv1062852
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)dgv3502n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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