A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv272n100



Internal ID20151888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109683008..109710508hg38UCSC Ensembl
chr1:110225630..110253130hg19UCSC Ensembl
chr1:110027153..110054653hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3827501
hg1927501
hg1827501
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1005433, nsv1010300, nsv1009135, nsv1013141, nsv1008557
Samples
Known GenesGSTM1, GSTM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv272n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss8
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer