A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3425n100



Internal ID22789512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8684212..8768019hg38UCSC Ensembl
chr19:8794475..8878695hg19UCSC Ensembl
chr19:8655475..8739695hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3883808
hg1984221
hg1884221
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056395, nsv1061653
Samples
Known GenesACTL9, OR2Z1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3425n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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