A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv276n100



Internal ID19010644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109690340..109714002hg38UCSC Ensembl
chr1:110232962..110256624hg19UCSC Ensembl
chr1:110034485..110058147hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3823663
hg1923663
hg1823663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv998361, nsv998943, nsv1013915, nsv1008867
Samples
Known GenesGSTM1, GSTM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv276n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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