A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3626n100



Internal ID22789713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51746647..52125358hg38UCSC Ensembl
chr19:52249900..52628611hg19UCSC Ensembl
chr19:56941712..57320423hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38378712
hg19378712
hg18378712
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059924, nsv1057217, nsv1061029, nsv1062154, nsv1064732, nsv1057485, nsv1061100, nsv1056146, nsv1060988, nsv1063940, nsv1060519, nsv1059263, nsv1058292, nsv1057290
Samples
Known GenesFPR1, FPR2, FPR3, HCCAT3, ZNF350, ZNF432, ZNF577, ZNF613, ZNF614, ZNF615, ZNF616, ZNF649, ZNF841
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3626n100
Frequency
Sample Size11257
Observed Gain27
Observed Loss0
Observed Complex0
Frequencyn/a


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