A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4909n100



Internal ID22790996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140188330..140223611hg38UCSC Ensembl
chr3:139907172..139942453hg19UCSC Ensembl
chr3:141389862..141425143hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3835282
hg1935282
hg1835282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003141, nsv1008578
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)dgv4909n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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