A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4672n100



Internal ID22790759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:6599013..6613379hg38UCSC Ensembl
chr3:6640700..6655066hg19UCSC Ensembl
chr3:6615700..6630066hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3814367
hg1914367
hg1814367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003296, nsv1014299, nsv1005576
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)dgv4672n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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