A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4644n100



Internal ID22790731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4038014..4210583hg38UCSC Ensembl
chr3:4079698..4252267hg19UCSC Ensembl
chr3:4054698..4227267hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38172570
hg19172570
hg18172570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010712, nsv1013595, nsv1007106, nsv1003424, nsv1005937
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4644n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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