A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4738n100



Internal ID20156354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46790459..46827326hg38UCSC Ensembl
chr3:46831949..46868816hg19UCSC Ensembl
chr3:46806953..46843820hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3836868
hg1936868
hg1836868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012921, nsv1010400
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)dgv4738n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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