A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4770n100



Internal ID22790857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68402059..68425978hg38UCSC Ensembl
chr3:68451209..68475128hg19UCSC Ensembl
chr3:68533899..68557818hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3823920
hg1923920
hg1823920
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1001320, nsv1006007
Samples
Known GenesFAM19A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4770n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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