A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4910n100



Internal ID22790997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140298157..140470306hg38UCSC Ensembl
chr3:140016999..140189148hg19UCSC Ensembl
chr3:141499689..141671838hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38172150
hg19172150
hg18172150
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004500, nsv1001430
Samples
Known GenesCLSTN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4910n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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