A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4600n100



Internal ID22790687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18655..46285hg38UCSC Ensembl
chr3:60333..87967hg19UCSC Ensembl
chr3:35333..62967hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3827631
hg1927635
hg1827635
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011542, nsv997464
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)dgv4600n100
Frequency
Sample Size11257
Observed Gain19
Observed Loss6
Observed Complex0
Frequencyn/a


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