A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3457n100



Internal ID22789544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19978057..20619795hg38UCSC Ensembl
chr19:20088866..20802601hg19UCSC Ensembl
chr19:19949866..20594441hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38641739
hg19713736
hg18644576
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1055694, nsv1064400
Samples
Known GenesMIR1270-1, MIR1270-2, ZNF486, ZNF682, ZNF737, ZNF826P, ZNF90
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3457n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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