A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4992n100



Internal ID22791079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:176175294..176231852hg38UCSC Ensembl
chr3:175893082..175949640hg19UCSC Ensembl
chr3:177375776..177432334hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3856559
hg1956559
hg1856559
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010036, nsv1010254, nsv1009642
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)dgv4992n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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