A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv260n100



Internal ID20151876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109676374..109694313hg38UCSC Ensembl
chr1:110218996..110236935hg19UCSC Ensembl
chr1:110020519..110038458hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3817940
hg1917940
hg1817940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006541, nsv1009780, nsv1012822
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)dgv260n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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