A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4901n100



Internal ID22790988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132266202..132284546hg38UCSC Ensembl
chr3:131985046..132003390hg19UCSC Ensembl
chr3:133467736..133486080hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3818345
hg1918345
hg1818345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1014220, nsv1002969, nsv1012530
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)dgv4901n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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