A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4737n100



Internal ID20156353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46770667..46818330hg38UCSC Ensembl
chr3:46812157..46859820hg19UCSC Ensembl
chr3:46787161..46834824hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3847664
hg1947664
hg1847664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1013563, nsv1000772
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)dgv4737n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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