A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5039n100



Internal ID22791126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:197180861..197242896hg38UCSC Ensembl
chr3:196907732..196969767hg19UCSC Ensembl
chr3:198392129..198454164hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3862036
hg1962036
hg1862036
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007354, nsv1002102
Samples
Known GenesDLG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5039n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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