A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4923n100



Internal ID22791010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152624726..152638401hg38UCSC Ensembl
chr3:152342515..152356190hg19UCSC Ensembl
chr3:153825205..153838880hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3813676
hg1913676
hg1813676
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv998978, nsv1011010, nsv1006438
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)dgv4923n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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