A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3586n100



Internal ID22789673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43037255..43109111hg38UCSC Ensembl
chr19:43541407..43613263hg19UCSC Ensembl
chr19:48233247..48305103hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3871857
hg1971857
hg1871857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060563, nsv1063755, nsv1064135, nsv1058364, nsv1059987, nsv1055500, nsv1062590, nsv1063619
Samples
Known GenesPSG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3586n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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